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
PubChem Substance ID:
UNSPSC Code:
12352209
Beilstein/REAXYS Number:
2115614
MDL number:
产品名称
Boc-4-Abz-OH, ≥98.0% (T)
SMILES string
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
assay
≥98.0% (T)
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
~200 °C (dec.)
application(s)
peptide synthesis
Other Notes
PABA 的 BOC 保护衍生物。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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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