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关于此项目
线性分子式:
ClC6H4NHCO2C(CH3)3
化学文摘社编号:
分子量:
227.69
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
assay
97%
mp
102-106 °C (lit.)
functional group
amine, chloro
SMILES string
CC(C)(C)OC(=O)Nc1ccc(Cl)cc1
InChI
1S/C11H14ClNO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14)
InChI key
VFEHOBXXLPHSOI-UHFFFAOYSA-N
Application
4-Chloro-(N-Boc)aniline may be used in the synthesis of:
- 4-[[9–chloro-7-(2,6-difluorophenyl)-5H-pyrimido[5,4-d][2]benzazepin-2-yl]-amino] benzoic acid(MLN8054)
- 5-(4-aminophenyl)-3H-1,2-dithiol-3-thione
- (E)(4(prop-1-en-1-yl)phenyl)carbamate
存储类别
13 - Non 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
Matthew D Hammers et al.
Synlett : accounts and rapid communications in synthetic organic chemistry, 27(9), 1349-1353 (2016-07-12)
As additional physiological functions of hydrogen sulfide (H
Bioorthogonal imaging of aurora kinase A in live cells.
Katherine S Yang et al.
Angewandte Chemie (International ed. in English), 51(27), 6598-6603 (2012-05-31)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 554162-25G | 04061832582320 |