226289
N,N-Dimethyltrimethylsilylamine
97%
동의어(들):
(Dimethylamino)trimethylsilane, N-(Trimethylsilyl)dimethylamine, TMSDMA
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모든 사진(1)
About This Item
Linear Formula:
(CH3)3SiN(CH3)2
CAS Number:
Molecular Weight:
117.26
Beilstein:
1731861
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
97%
양식
liquid
refractive index
n20/D 1.397 (lit.)
bp
84 °C (lit.)
density
0.732 g/mL at 25 °C (lit.)
작용기
amine
SMILES string
CN(C)[Si](C)(C)C
InChI
1S/C5H15NSi/c1-6(2)7(3,4)5/h1-5H3
InChI key
KAHVZNKZQFSBFW-UHFFFAOYSA-N
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애플리케이션
N,N-Dimethyltrimethylsilylamine can be used as a reactant to prepare:
It can also be used as a silylating agent in chemical synthesis.
- Trifluoromethylacetophenone-N,N-dimethyltrimethylsilylamine adduct, which is used as an efficient reagent for nucleophilic trifluoromethylation of carbonyl and the imine group.
- (Dimethylamino)sulfur trifluoride (Me-DAST), which is employed as a deoxofluorinating agent for the conversion of aliphatic alcohols into their corresponding fluorides.
- Nucleoside phosphoramidites by reacting with alkyloxy (or aryloxy)-triazolylphosphine and deoxynucleoside.
It can also be used as a silylating agent in chemical synthesis.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - Water-react 1
Storage Class Code
4.3 - Hazardous materials which set free flammable gases upon contact with water
WGK
WGK 3
Flash Point (°F)
10.4 °F - closed cup
Flash Point (°C)
-12 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Tetrahedron Letters, 34, 5863-5863 (1993)
A new and general procedure for the preparation of deoxynucleoside phosphoramidites.
Fourrey JL and Varenne J.
Tetrahedron Letters, 24(19), 1963-1966 (1983)
Tetrahedron, 49, 2299-2299 (1993)
J. Photopolym. Sci. Technol., 5, 123-123 (1992)
A new and general procedure for the preparation of deoxynucleoside phosphoramidites
Fourrey J-L and Varenne J
Tetrahedron Letters, 24(19), 1963-1966 (1983)
문서
Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs
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