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3277-26-7 molecular structure
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[(dimethylsilyl)oxy]dimethylsilane

ChemBase ID: 112784
Molecular Formular: C4H14OSi2
Molecular Mass: 134.32436
Monoisotopic Mass: 134.05831813
SMILES and InChIs

SMILES:
C[SiH](C)O[SiH](C)C
Canonical SMILES:
C[SiH](O[SiH](C)C)C
InChI:
InChI=1S/C4H14OSi2/c1-6(2)5-7(3)4/h6-7H,1-4H3
InChIKey:
NVYQDQZEMGUESH-UHFFFAOYSA-N

Cite this record

CBID:112784 http://www.chembase.cn/molecule-112784.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[(dimethylsilyl)oxy]dimethylsilane
IUPAC Traditional name
dimethylsilyl ether
Synonyms
1,1,3,3-TETRAMETHYLDISILOXANE
Siloxane HSi2
1,1,3,3-Tetramethyldisiloxane
四甲基二氢二硅氧烷
1,1,3,3-四甲基二硅氧烷
1,1,3,3-四甲基二甲硅醚
CAS Number
3277-26-7
EC Number
221-906-4
MDL Number
MFCD00008256
Beilstein Number
1733364
PubChem SID
24889321
24900267
162097975
24853998
24888743
PubChem CID
6327482

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) -0.1864  LogD (pH = 7.4) -0.1864 
Log P -0.1864  Molar Refractivity 26.0706 cm3
Polarizability 14.659903 Å3 Polar Surface Area 9.23 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
-78°C expand Show data source
Boiling Point
70-71 °C(lit.) expand Show data source
70-71°C expand Show data source
Flash Point
-14.8 °F expand Show data source
-26 °C expand Show data source
-26°C(-15°F) expand Show data source
Density
0.76 g/mL at 25 °C(lit.) expand Show data source
0.760 expand Show data source
Refractive Index
1.3700 expand Show data source
n20/D 1.370 expand Show data source
n20/D 1.370(lit.) expand Show data source
Storage Warning
Moisture Sensitive expand Show data source
RTECS
JN1000000 expand Show data source
European Hazard Symbols
Flammable Flammable (F) expand Show data source
UN Number
1993 expand Show data source
UN1993 expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
2 expand Show data source
Hazard Class
3 expand Show data source
Packing Group
2 expand Show data source
II expand Show data source
Risk Statements
11 expand Show data source
11-16 expand Show data source
Safety Statements
16 expand Show data source
9-16-29-33 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS02 expand Show data source
GHS Signal Word
Danger expand Show data source
GHS Hazard statements
H225 expand Show data source
GHS Precautionary statements
P210 expand Show data source
P210-P243-P403+P233 expand Show data source
Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter expand Show data source
RID/ADR
UN 1993 3/PG 2 expand Show data source
Storage Temperature
2-8°C expand Show data source
Purity
≥97% expand Show data source
≥97.0% (GC) expand Show data source
≥98.0% (GC) expand Show data source
97% expand Show data source
Grade
produced by Wacker expand Show data source
purum expand Show data source
Certificate of Analysis
Download expand Show data source
Linear Formula
[(CH3)2SiH]2O expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich
MP Biomedicals - 05225814 external link
MP Biomedicals Rare Chemical collection
Sigma Aldrich - 92231 external link
Other Notes
prices for bulk quantities on request
Packaging
500 g in glass bottle
Sigma Aldrich - 235733 external link
Packaging
25, 100 g in glass bottle
Sigma Aldrich - 87835 external link
Other Notes
Reducing agent1,2,3

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Reducing agent:
  • • In the presence of TMS chloride and either LiBr or NaI, aromatic aldehydes are reduced directly to benzyl halides: Tetrahedron Lett., 25, 1103 (1984).
  • • With a Pd(0) catalyst, acetylenes are reduced to olefins (mainly cis): Tetrahedron Lett., 30, 4675 (1989).
  • • Forms polymers via hydrosilylation of alkadienes and and alkynes.
  • • In the presence of a catalytic amount of titanium isopropoxide, secondary and tertiary phosphine oxides can be reduced to the corresponding phosphines in high yield, avoiding pyrophoric reagents: Synlett, 1545 (2007).
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PATENTS

PATENTS

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INTERNET

INTERNET

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