15299
Boc-4-Abz-OH
≥98.0% (T)
别名:
4-(叔丁氧羰基氨基)苯甲酸
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关于此项目
线性分子式:
(CH3)3CO2CNHC6H4CO2H
化学文摘社编号:
分子量:
237.25
Beilstein:
2115614
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
方案
≥98.0% (T)
反应适用性
reaction type: Boc solid-phase peptide synthesis
mp
~200 °C (dec.)
应用
peptide synthesis
SMILES字符串
CC(C)(C)OC(=O)Nc1ccc(cc1)C(O)=O
InChI
1S/C12H15NO4/c1-12(2,3)17-11(16)13-9-6-4-8(5-7-9)10(14)15/h4-7H,1-3H3,(H,13,16)(H,14,15)
InChI key
ZJDBQMWMDZEONW-UHFFFAOYSA-N
其他说明
PABA 的 BOC 保护衍生物。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
M H Norman et al.
Journal of medicinal chemistry, 39(5), 1172-1188 (1996-03-01)
A series of substituted (4-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)butyl)benzamide derivatives was prepared and evaluated as potential atypical antipsychotic agents. The target compounds were readily prepared from their benzoyl chloride, benzoic acid, or isatoic anhydride precursors, and they were evaluated in vitro for their ability
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