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Details

Stereochemistry ACHIRAL
Molecular Formula C6H19NSi2
Molecular Weight 161.3928
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEXAMETHYLDISILAZANE

SMILES

C[Si](C)(C)N[Si](C)(C)C

InChI

InChIKey=FFUAGWLWBBFQJT-UHFFFAOYSA-N
InChI=1S/C6H19NSi2/c1-8(2,3)7-9(4,5)6/h7H,1-6H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and characterization of endcapped C18 stationary phases using a silica hydride intermediate.
2002 Feb 22
Analogues of thiolactomycin: potential drugs with enhanced anti-mycobacterial activity.
2002 Oct
Synthesis of 11C-amides using [11C]carbon monoxide and in situ activated amines by palladium-mediated carboxaminations.
2003 Feb 7
Structural studies of N,N'-di(ortho-fluorophenyl)formamidine group 1 metallation.
2003 Jan 20
Determination of the absolute structure of (+)-cystothiazole B.
2004 Jun
Unprecedented catalytic asymmetric reduction of N-H imines.
2005 Jan 20
Base-promoted acyloin rearrangement of 1,8-di-tert-butyldimethylsilyloxybicyclo[2.2.2]oct-5-en-2-ones.
2005 Jun
C-H Activation (gamma-deprotonation) of a Sm(III) bis(trimethylsilyl)amide complex via macrocyclic stabilisation of the sodium counter ion.
2005 Mar 28
FeSO4 x 7H2O-catalyzed four-component synthesis of protected homoallylic amines.
2007 Jul 6
Silica passivation efficiency monitored by a surface-bound fluorescent dye.
2008 Aug 19
Displayed correlation between gene expression profiles and submicroscopic alterations in response to cetuximab, gefitinib and EGF in human colon cancer cell lines.
2008 Aug 8
pH-responsive biodegradable micelles based on acid-labile polycarbonate hydrophobe: synthesis and triggered drug release.
2009 Jul 13
Beta-diketiminato calcium and magnesium amides; model complexes for hydroamination catalysis.
2009 May 18
Solid-state (49/47)Ti NMR of titanium-based MCM-41 hybrid materials.
2009 Nov 3
Patents
Name Type Language
HEXAMETHYLDISILAZANE
HSDB   MI  
Systematic Name English
HEXAMETHYLDISILAZANE [MI]
Common Name English
NSC-93895
Code English
1,1,1-TRIMETHYL-N-(TRIMETHYLSILYL)SILANAMINE
Systematic Name English
HEXAMETHYLDISILAZANE [HSDB]
Common Name English
Code System Code Type Description
SMS_ID
100000170857
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
PRIMARY
ECHA (EC/EINECS)
213-668-5
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
PRIMARY
CAS
999-97-3
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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NSC
93895
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
PRIMARY
CHEBI
85068
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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DAILYMED
H36C68P1BH
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
PRIMARY
EVMPD
SUB185133
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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RXCUI
1986434
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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EPA CompTox
DTXSID2025395
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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MESH
C024548
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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WIKIPEDIA
Bis(trimethylsilyl)amine
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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PUBCHEM
13838
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
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FDA UNII
H36C68P1BH
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
PRIMARY
HSDB
7226
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
PRIMARY
MERCK INDEX
m5995
Created by admin on Fri Dec 15 18:26:04 GMT 2023 , Edited by admin on Fri Dec 15 18:26:04 GMT 2023
PRIMARY Merck Index