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1 G
$144.00
About This Item
线性分子式:
(C8H6N)B(OH)2
CAS号:
分子量:
160.97
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
≥95%
表单
powder
mp
177-181 °C
储存温度
2-8°C
SMILES字符串
OB(O)c1ccc2cc[nH]c2c1
InChI
1S/C8H8BNO2/c11-9(12)7-2-1-6-3-4-10-8(6)5-7/h1-5,10-12H
InChI key
ZVMHOIWRCCZGPZ-UHFFFAOYSA-N
应用
用于研究在 Suzuki 交叉偶联反应中，芳氨基酸的外消旋作用。[1]
Reactant involved in synthesis of:
Reactant involved in Suzuki-Miyaura reactions
- Indole compounds for use as HIV-1 glycoprotein-41 fusion inhibitors
- δ-Carbolines / carbozoles
- Trisubstituted pyrimidines as PI3K inhibitors
- (Thienopyridine)carboxamides as CHK1 inhibitors
- cis-Fluorostilbenes
Reactant involved in Suzuki-Miyaura reactions
其他说明
可能含有不定量的酸酐
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Monica Prieto et al.
The Journal of organic chemistry, 72(3), 1047-1050 (2007-01-27)
Reaction conditions considered to be typical in Suzuki couplings can cause significant (up to 34% of the unwanted enantiomer) loss of optical purity in sensitive substrates such as hydroxyphenylglycine 1. This may be remedied using sodium succinate instead of sodium
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