12039-83-7|Titanium silicide|Titanium disilicide|(λ2-silanylidenetitaniumylidene)-λ...

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(λ²-silanylidenetitaniumylidene)-λ²-silanylidene: ChemBase ID: 129925; Molecular Formular: Si2Ti; Molecular Mass: 104.038; Monoisotopic Mass: 103.90179936
SMILES and InChIs

SMILES:
[Si]=[Ti]=[Si]
Canonical SMILES:
[Si]=[Ti]=[Si]
InChI:
InChI=1S/2Si.Ti
InChIKey:
DFJQEGUNXWZVAH-UHFFFAOYSA-N
Cite this record CBID:129925 http://www.chembase.cn/molecule-129925.html

NAMES AND DATABASE IDS

Names Database IDs

IUPAC name

(λ²-silanylidenetitaniumylidene)-λ²-silanylidene

IUPAC Traditional name

(λ²-silanylidenetitaniumylidene)-λ²-silanylidene

Synonyms

Titanium silicide

Titanium disilicide

Titanium silicide sputtering target, 50.8mm (2.0in) dia x 6.35mm (0.250in) thick

Titanium silicide sputtering target, 76.2mm (3.0in) dia x 3.18mm (0.125in) thick

Titanium silicide

Titanium silicide sputtering target, 50.8mm (2.0in) dia x 3.18mm (0.125in) thick

Titanium silicide sputtering target, 76.2mm (3.0in) dia x 6.35mm (0.250in) thick

硅化钛溅射靶, 50.8mm (2.0in) 直径 x 6.35mm (0.250in) 厚

硅化钛溅射靶, 76.2mm (3.0in) 直径 x 3.18mm (0.125in) 厚

硅化钛

硅化钛溅射靶, 50.8mm (2.0in) 直径 x 3.18mm (0.125in) 厚

硅化钛溅射靶, 76.2mm (3.0in) 直径 x 6.35mm (0.250in) 厚

CAS Number

12039-83-7

EC Number

234-904-3

235-082-9

MDL Number

MFCD00151541

PubChem SID

162224211

PubChem CID

6336889

Wikipedia Title

Titanium_disilicide

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources

Data Source	Data ID
Alfa Aesar	41114 41117 41115 41116 13088
Wikipedia	Titanium_disilicide
PubChem	6336889

Data Source

Data ID

Price

Alfa Aesar

41114	Please log in.
41117	Please log in.
41115	Please log in.
41116	Please log in.
13088	Please log in.

Data Source	Data ID
Wikipedia	Titanium_disilicide
PubChem	6336889

CALCULATED PROPERTIES

JChem

H Acceptors	0	H Donor	0
LogD (pH = 5.5)	0.09	LogD (pH = 7.4)	0.09
Log P	0.09	Molar Refractivity	0.0 cm³
Polarizability	7.3789454 Å³	Polar Surface Area	0.0 Å²
Rotatable Bonds	0	Lipinski's Rule of Five	true

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)

Solubility

insoluble in water	Show data source Wikipedia.org - Titanium_disilicide
soluble in HF	Show data source Wikipedia.org - Titanium_disilicide

Apperance

-325 Mesh Powder	Show data source Alfa Aesar - 13088
black orthorhombic crystals	Show data source Wikipedia.org - Titanium_disilicide

Melting Point

1470°C	Show data source Wikipedia.org - Titanium_disilicide
1760°C	Show data source Alfa Aesar - 13088

Density

4.02 g/cm³

Show data source

European Hazard Symbols

Flammable (F)	Show data source Alfa Aesar - 13088
Irritant (Xi)	Show data source Alfa Aesar - 13088

UN Number

UN3178

Show data source

Hazard Class

4.1	Show data source Alfa Aesar - 13088

Packing Group

III	Show data source Alfa Aesar - 13088

Risk Statements

11-36/37/38

Show data source

Safety Statements

26-37

Show data source

TSCA Listed

是	Show data source Alfa Aesar - 13088 Alfa Aesar - 41114 Alfa Aesar - 41115 Alfa Aesar - 41116 Alfa Aesar - 41117

GHS Pictograms

	Show data source Alfa Aesar - 13088
	Show data source Alfa Aesar - 13088

GHS Hazard statements

H228-H315-H319-H335

Show data source

GHS Precautionary statements

P210-P241-P305+P351+P338-P302+P352-P405-P501A

Show data source

Purity

99.5% (metals basis)

Show data source

DETAILS

Wikipedia

Wikipedia.org - Titanium_disilicide

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

(λ2-silanylidenetitaniumylidene)-λ2-silanylidene

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

(λ²-silanylidenetitaniumylidene)-λ²-silanylidene