364649
tert-Butylmagnesium chloride solution
1.0 M in THF
동의어(들):
t-Butylmagnesium chloride, tert-Butylchloromagnesium, Chloro(1,1-dimethylethyl)magnesium
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모든 사진(1)
About This Item
Linear Formula:
(CH3)3CMgCl
CAS Number:
Molecular Weight:
116.87
Beilstein:
3535403
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
반응 적합성
reaction type: Grignard Reaction
농도
1.0 M in THF
density
0.931 g/mL at 25 °C
SMILES string
CC(C)(C)[Mg]Cl
InChI
1S/C4H9.ClH.Mg/c1-4(2)3;;/h1-3H3;1H;/q;;+1/p-1
InChI key
ZDRJSYVHDMFHSC-UHFFFAOYSA-M
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일반 설명
tert-Butylmagnesium chloride, an organomagnesium compound, is commonly known as Grignard reagent. It is a powerful carbon nucleophile mainly used for C-C bond formation.
애플리케이션
tert-Butylmagnesium chloride (1.0 M in THF) has been used in the preparation of tert-butylsulfinyl chloride.
It can be used in:
It can be used in:
- Grignard metathesis reaction of 2,5-dibromo-3-hexylthiophene to form 2-bromo-5-magnesiobromo-3-hexylthiophene.
- A key step for the asymmetric synthesis of sulfinyl transfer agents using cinchona alkaloids quinine and quinidine as chiral auxiliaries.
기타 정보
Storage below 25°C may cause formation of crystalline magnesium salts. Moving container to a warm location and ocassional gentle swirling should redissolve the solid.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Skin Corr. 1B - STOT SE 3 - Water-react 1
표적 기관
Respiratory system
보충제 위험성
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 3
Flash Point (°F)
1.4 °F - closed cup
Flash Point (°C)
-17 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Organic Chemistry, 542-542 (2008)
New general sulfinylating process for asymmetric synthesis of enantiopure sulfinates and sulfoxides.
Lu B Z, et al.
Organic Letters, 7(8), 1465-1468 (2005)
"Tert-butylsulfonyl (Bus), a new protecting group for amines"
Sun P, et al.
The Journal of Organic Chemistry, 62(24), 8604-8608 (1997)
Facile synthesis of end-functionalized regioregular poly (3-alkylthiophene) s via modified Grignard metathesis reaction.
Jeffries-El M, et al.
Macromolecules, 38(25), 10346-10352 (2005)
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