14275-61-7|trans-1,2-Bis(tributylstannyl)ethene|trans-1,2-Bis(tributylstannyl)eth...

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tributyl[2-(tributylstannyl)ethenyl]stannane: ChemBase ID: 64241; Molecular Formular: C26H56Sn2; Molecular Mass: 606.12484; Monoisotopic Mass: 608.24258979
SMILES and InChIs

SMILES:
C(=C\[Sn](CCCC)(CCCC)CCCC)/[Sn](CCCC)(CCCC)CCCC
Canonical SMILES:
CCCC[Sn](/C=C/[Sn](CCCC)(CCCC)CCCC)(CCCC)CCCC
InChI:
InChI=1S/6C4H9.C2H2.2Sn/c6*1-3-4-2;1-2;;/h6*1,3-4H2,2H3;1-2H;;
InChIKey:
VNKOWRBFAJTPLS-UHFFFAOYSA-N
Cite this record CBID:64241 http://www.chembase.cn/molecule-64241.html

NAMES AND DATABASE IDS

Names Database IDs

IUPAC name

tributyl[2-(tributylstannyl)ethenyl]stannane

tributyl[(E)-2-(tributylstannyl)ethenyl]stannane

IUPAC Traditional name

tributyl[2-(tributylstannyl)ethenyl]stannane

tributyl[(E)-2-(tributylstannyl)ethenyl]stannane

Synonyms

trans-1,2-Bis(tributylstannyl)ethylene

trans-1,2-Bis(tributylstannyl)ethene

trans-1,2-Bis(tri-n-butylstannyl)ethylene

trans-1,2-Bis(tributylstannyl)ethene

反-1,2-双(三正丁基锡)乙烯

CAS Number

14275-61-7

MDL Number

MFCD01631299

Beilstein Number

3613803

PubChem SID

162029980

PubChem CID

5378370

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources

Data Source	Data ID
Sigma Aldrich	731625
Alfa Aesar	L20130
Matrix Scientific	069567
Apollo Scientific	OR15601
PubChem	5378370

Data Source

Data ID

Price

Sigma Aldrich

731625

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Alfa Aesar

L20130

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Matrix Scientific

069567

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Apollo Scientific

OR15601

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Data Source	Data ID
PubChem	5378370

CALCULATED PROPERTIES

JChem

H Acceptors	0	H Donor	0
LogD (pH = 5.5)	13.093	LogD (pH = 7.4)	13.093
Log P	13.093	Molar Refractivity	125.8202 cm³
Polarizability	59.02428 Å³	Polar Surface Area	0.0 Å²
Rotatable Bonds	20	Lipinski's Rule of Five	false

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)

Boiling Point

185°C/0.01mm

Show data source

Flash Point

>110 °C	Show data source Sigma Aldrich - 731625
>230 °F	Show data source Sigma Aldrich - 731625

Density

1.132 g/mL at 25 °C	Show data source Sigma Aldrich - 731625
1.140	Show data source Alfa Aesar - L20130

Refractive Index

1.5020	Show data source Alfa Aesar - L20130
n20/D 1.502	Show data source Sigma Aldrich - 731625

Storage Warning

Air & Moisture Sensitive	Show data source Alfa Aesar - L20130
IRRITANT	Show data source Matrix Scientific - 069567
Toxic	Show data source Apollo Scientific Ltd - OR15601

European Hazard Symbols

Nature polluting (N)	Show data source Sigma Aldrich - 731625 Alfa Aesar - L20130
Toxic (T)	Show data source Sigma Aldrich - 731625 Alfa Aesar - L20130

UN Number

UN2788

Show data source

MSDS Link

Download	Show data source Matrix Scientific - 069567
Download	Show data source Sigma Aldrich - 731625

German water hazard class

3	Show data source Sigma Aldrich - 731625

Hazard Class

6.1	Show data source Alfa Aesar - L20130

Packing Group

II	Show data source Alfa Aesar - L20130

Risk Statements

21-25-36/38-48/23/25-50/53

Show data source

Safety Statements

35-36/37/39-45-60-61	Show data source Alfa Aesar - L20130
36/37/39-45-60-61	Show data source Sigma Aldrich - 731625

TSCA Listed

false	Show data source Matrix Scientific - 069567
否	Show data source Alfa Aesar - L20130

GHS Pictograms

	Show data source Sigma Aldrich - 731625 Alfa Aesar - L20130
	Show data source Sigma Aldrich - 731625 Alfa Aesar - L20130
	Show data source Sigma Aldrich - 731625 Alfa Aesar - L20130

GHS Signal Word

Danger

Show data source

GHS Hazard statements

H300-H311-H315-H319-H372-H400-H410	Show data source Alfa Aesar - L20130
H301-H312-H315-H319-H372-H410	Show data source Sigma Aldrich - 731625

GHS Precautionary statements

P260-P301+P310-P305+P351+P338-P361-P405-P501A	Show data source Alfa Aesar - L20130
P273-P280-P301 + P310-P305 + P351 + P338-P314-P501	Show data source Sigma Aldrich - 731625

Storage Temperature

2-8°C

Show data source

Purity

90%	Show data source Matrix Scientific - 069567
96%	Show data source Alfa Aesar - L20130
97%	Show data source Sigma Aldrich - 731625

Empirical Formula (Hill Notation)

C26H56Sn2

Show data source

DETAILS

Sigma Aldrich

Sigma Aldrich - 731625

Packaging
1, 5 g in glass bottle

REFERENCES

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PATENTS

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INTERNET

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Part I: Carbon
- I.1: Carbon-Carbon Bonds
- I.1.1 Alkanes
- Primary carbon
- Secondary carbon
- Tertiary carbon
- Quaternary carbon
- I.1.2 C-C double and Triple Bonds
- Alkene
- Alkyne
- Allene
- I.2: One Carbon-Hetero Bond
- I.2.1 Alkyl Halogenides
- Alkylchloride
- Alkylfluoride
- Alkylbromide
- Alkyliodide
- I.2.2 Alcohols and Ethers
- Alcohol
- Primary alcohol
- Secondary alcohol
- Tertiary alcohol
- Dialkylether
- Dialkylthioether
- Alkylarylether
- Diarylether
- Alkylarylthioether
- Diarylthioether
- Oxonium
- I.2.3 Amines
- Amine
- Primary aliphatic amine
- Secondary aliphatic amine
- Tertiary aliphatic amine
- Quaternary aliphatic ammonium
- Primary aromatic amine
- Secondary aromatic amine
- Tertiary aromatic amine
- Quaternary aromatic ammonium
- Secondary mixed amine
- Tertiary mixed amine
- Quaternary mixed ammonium
- Ammonium
- I.2.4 Others
- Alkylthiol
- Dialkylthioether
- Alkylarylthioether
- Disulfide
- 1,2-Aminoalcohol
- 1,2-Diol
- 1,1-Diol
- Hydroperoxide
- Peroxo
- Organolithium compounds
- Organomagnesium compounds
- Organometallic compounds
- I.3: Two Carbon-Hetero Bonds (Carbonyl and Derivatives)
- I.3.1 Double Bond to Hetero
- Aldehyde
- Ketone
- Thioaldehyde
- Thioketone
- Imine
- Immonium
- Oxime
- Oximether
- I.3.2. Two Single Bonds to Hetero
- Acetal
- Hemiacetal
- Aminal
- Hemiaminal
- Thioacetal
- Thiohemiacetal
- Halogen acetal like
- Acetal like
- Halogenmethylen ester and similar
- NOS methylen ester and similar
- Hetero methylen ester and similar
- Cyanhydrine
- I.3.3 Single Bond to Hetero, C=C Double Bond (Enols and Similar)
- Chloroalkene
- Fluoroalkene
- Bromoalkene
- Iodoalkene
- Enol
- Endiol
- Enolether
- Enolester
- Enamine
- Thioenol
- Thioenolether
- I.4: Three Carbon-Hetero Bonds (Carboxyl and Derivatives)
- Acylchloride
- Acylfluoride
- Acylbromide
- Acyliodide
- Acylhalide
- Carboxylic acid
- Carboxylic ester
- Lactone
- Carboxylic anhydride
- Carboxylic acid derivative
- Carbothioic acid
- Carbothioic S ester
- Carbothioic S lactone
- Carbothioic O ester
- Carbothioic O lactone
- Carbothioic halide
- Carbodithioic acid
- Carbodithioic ester
- Carbodithiolactone
- Amide
- Primary amide
- Secondary amide
- Tertiary amide
- Lactam
- Alkyl imide
- N hetero imide
- Imide acidic
- Thioamide
- Thiolactam
- Oximester
- Amidine
- Hydroxamic acid
- Hydroxamic acid ester
- Imidoacid
- Imidoacid cyclic
- Imidoester
- Imidolactone
- Imidothioacid
- Imidothioacid cyclic
- Imidothioester
- Imidothiolactone
- Amidine
- Imidolactam
- Imidoylhalide
- Imidoylhalide cyclic
- Amidrazone
- Alpha aminoacid
- Alpha hydroxyacid
- Peptide middle
- Peptide C term
- Peptide N term
- Carboxylic orthoester
- Ketene
- Ketenacetal
- Nitrile
- Isonitrile
- Vinylogous carbonyl or carboxyl derivative
- Vinylogous acid
- Vinylogous ester
- Vinylogous amide
- Vinylogous halide
- I.5: Four Carbon-Hetero Bonds (Carbonic Acid and Derivatives)
- Carbonic acid dieester
- Carbonic acid esterhalide
- Carbonic acid monoester
- Carbonic acid derivatives
- Thiocarbonic acid dieester
- Thiocarbonic acid esterhalide
- Thiocarbonic acid monoester
- Urea
- Thiourea
- Isourea
- Isothiourea
- Guanidine
- Carbaminic acid
- Urethan(Carbamate ester)
- Biuret
- Semicarbazide
- Carbazide
- Semicarbazone
- Carbazone
- Thiosemicarbazide
- Thiocarbazide
- Thiosemicarbazone
- Thiocarbazone
- Isocyanate
- Cyanate
- Isothiocyanate
- Thiocyanate
- Carbodiimide
- Orthocarbonic derivatives
- I.6 Aromatics
- Phenol
- 1,2-Diphenol
- Arylchloride
- Arylfluoride
- Arylbromide
- Aryliodide
- Arylthiol
- Iminoarene
- Oxoarene
- Thioarene
- Hetero N basic H
- Hetero N basic no H
- Hetero N nonbasic
- Hetero O
- Hetero S
- Heteroaromatic
Part II: N, S, P, Si, B
- II.1 Nitrogen
- Nitrite
- Thionitrite
- Nitrate
- Nitro
- Nitroso
- Azide
- Acylazide
- Diazo
- Diazonium
- Nitrosamine
- Nitrosamide
- N-Oxide
- Hydrazine
- Hydrazone
- Hydroxylamine
- II.2 Sulfur
- Sulfon
- Sulfoxide
- Sulfonium
- Sulfuric acid
- Sulfuric monoester
- Sulfuric diester
- Sulfuric monoamide
- Sulfuric diamide
- Sulfuric esteramide
- Sulfuric derivative
- Sulfonic acid
- Sulfonamide
- Sulfonic ester
- Sulfonic halide
- Sulfonic derivative
- Sulfinic acid
- Sulfinic amide
- Sulfinic ester
- Sulfinic halide
- Sulfinic derivative
- Sulfenic acid
- Sulfenic amide
- Sulfenic ester
- Sulfenic halide
- Sulfenic derivative
- II.3 Phosphorous
- Phosphine
- Phosphine oxide
- Phosphonium
- Phosphorylen
- Phosphonic acid
- Phosphonic monoester
- Phosphonic diester
- Phosphonic monoamide
- Phosphonic diamide
- Phosphonic esteramide
- Phosphonic acid derivative
- Phosphoric acid
- Phosphoric monoester
- Phosphoric diester
- Phosphoric triester
- Phosphoric monoamide
- Phosphoric diamide
- Phosphoric triamide
- Phosphoric monoestermonoamide
- Phosphoric diestermonoamide
- Phosphoric monoesterdiamide
- Phosphoric acid derivative
- Phosphinic acid
- Phosphinic ester
- Phosphinic amide
- Phosphinic acid derivative
- Phosphonous acid
- Phosphonous monoester
- Phosphonous diester
- Phosphonous monoamide
- Phosphonous diamide
- Phosphonous esteramide
- Phosphonous derivatives
- Phosphinous acid
- Phosphinous ester
- Phosphinous amide
- Phosphinous derivatives
- II.4 Silicon
- Quart silane
- Non-quart silane
- Silylmonohalide
- Het trialkylsilane
- Dihet dialkylsilane
- Trihet alkylsilane
- Silicic acid derivative
- II.5 Boron
- Trialkylborane
- Boric acid derivatives
- Boronic acid derivative
- Borohydride
- Quaternary boron
Part III: Some Special Patterns
- III.1 Chains
- III.2 Rings
- Aromatic
- Heterocyclic
- Epoxide
- NH aziridine
- Spiro
- Annelated rings
- Bridged rings
- III.3 Sugars and Nucleosides/Nucleotides, Steroids
- Sugar pattern 1
- Sugar pattern 2
- Sugar pattern combi
- Sugar pattern 2 reducing
- Sugar pattern 2 alpha
- Sugar pattern 2 beta
- III.4 Everything else...
- Conjugated double bond
- Conjugated tripple bond
- Cis double bond
- Trans double bond
- Mixed anhydrides
- Halogen on hetero
- Halogen multi subst
- Trifluoromethyl
- C ONS bond
- Charged
- Anion
- Kation
- Salt
- 1,3-Tautomerizable
- 1,5-Tautomerizable
- Rotatable bond
- Michael acceptor
- Dicarbodiazene
- CH-acidic
- CH-acidic strong
- Chiral center specified

tributyl[2-(tributylstannyl)ethenyl]stannane

SMILES and InChIs

Cite this record

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

DATA SOURCES

DATA SOURCES

CALCULATED PROPERTIES

CALCULATED PROPERTIES

PROPERTIES

PROPERTIES

DETAILS

DETAILS

REFERENCES

REFERENCES

PATENTS

PATENTS

INTERNET

INTERNET