추천 제품
분석
97%
형태
liquid
refractive index
n20/D 1.397 (lit.)
bp
84 °C (lit.)
density
0.732 g/mL at 25 °C (lit.)
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
관련 카테고리
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
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
A new and general procedure for the preparation of deoxynucleoside phosphoramidites.
Tetrahedron Letters, 24(19), 1963-1966 (1983)
Tetrahedron, 49, 2299-2299 (1993)
Synthesis and evaluation of novel daunomycin-phosphate-sulfate-β-glucuronide and-β-glucoside prodrugs for application in ADEPT
Bioorganic & medicinal chemistry letters, 5(24), 2975-2980 (1995)
A new and general procedure for the preparation of deoxynucleoside phosphoramidites
Tetrahedron Letters, 24(19), 1963-1966 (1983)
Some studies on nucleophilic trifluoromethylation using the shelf-stable trifluoromethylacetophenone-N, N-dimethyltrimethylsilylamine adduct
Journal of Fluorine Chemistry, 126(4), 489-496 (2005)
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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