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About This Item
线性分子式:
BrCH2CH2CHBrCOCl
CAS号:
分子量:
264.34
Beilstein:
4955401
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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等級
technical
化驗
~90% (GC)
折射率
n20/D 1.535
密度
2.00 g/mL at 20 °C
儲存溫度
2-8°C
SMILES 字串
ClC(=O)C(Br)CCBr
InChI
1S/C4H5Br2ClO/c5-2-1-3(6)4(7)8/h3H,1-2H2
InChI 密鑰
WYZLYWUZERABRL-UHFFFAOYSA-N
應用
2,4-Dibromobutyryl chloride was used in the preparation of:
- methyl 2,4-dibromobutanoate
- series of 3-(3, 5-di-tert-butyl-4-hydroxybenzylidene)pyrrolidin-2-ones, anti-inflammatory/analgesic agents
- α-bromolactam
訊號詞
Danger
危險聲明
危險分類
Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1
安全危害
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Preparation of enantiopure 2-acylazetidines and their reactions with chloroformates.
Ma S, et al.
Tetrahedron Letters, 48(2), 269-271 (2007)
Bhooma Raghavan et al.
The Journal of organic chemistry, 71(5), 2151-2154 (2006-02-25)
A concise, stereoselective synthesis of alpha-substituted gamma-lactams is reported. gamma-Lactam scaffolds 2 and 3, possessing an Evans' chiral auxiliary and two types of N substituents, were successfully alkylated with different electrophiles to give alpha-substituted gamma-lactams with reasonable diastereoselectivities. The use
H Ikuta et al.
Journal of medicinal chemistry, 30(11), 1995-1998 (1987-11-01)
A series of 3-(3,5-di-tert-butyl-4-hydroxybenzylidene)pyrrolidin-2-ones was synthesized and evaluated as candidate antiinflammatory/analgesic agents as well as dual inhibitors of prostaglandin and leukotriene synthesis. Some compounds that showed dual inhibitory activity were found to possess equipotent antiinflammatory activities to indomethacin, with reduced
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