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About This Item
线性分子式:
BrCH2CHBrCOCl
CAS号:
分子量:
250.32
Beilstein:
1749801
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
推荐产品
化驗
97%
形狀
liquid
折射率
n20/D 1.542 (lit.)
bp
191-193 °C (lit.)
密度
2.181 g/mL at 25 °C (lit.)
SMILES 字串
ClC(=O)C(Br)CBr
InChI
1S/C3H3Br2ClO/c4-1-2(5)3(6)7/h2H,1H2
InChI 密鑰
HWKWYDXHMQQDQJ-UHFFFAOYSA-N
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應用
2,3-Dibromopropionyl chloride was used in synthesis of:
- series of 2,3-diaminopropionanilides
- enantiomers of 1,4-dideoxy-1,4-iminolyxitol and 1,4-dideoxy-1,4-iminoribitol
- acromelic acid A
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
150.8 °F - closed cup
閃點（°C）
66 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
P A Tenthorey et al.
Journal of medicinal chemistry, 24(9), 1059-1063 (1981-09-01)
A series of 2,3-diaminopropionanilides was synthesized by acylation of mono- and disubstituted aniline derivatives with 2,3-dibromopropionyl chloride and subsequent amination with the appropriate secondary amines. The target compounds were evaluated in mice for antiarrhythmic efficacy against chloroform-induced tachycardia and for
Concise enantioselective synthesis of acromelic acid A.
Takano S, et al.
Journal of the American Chemical Society, 109(18), 5523-5524 (1987)
Chiral synthesis of both enantiomers of 1, 4-dideoxy-1, 4-immolyxitol and 1, 4-dideoxy-1, 4-iminoribitol.
Takano S, et al.
Tetrahedron Asymmetry, 3(6), 681-684 (1992)
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