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About This Item
经验公式（希尔记法）:
C6H10ClNO
CAS号:
分子量:
147.60
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
方案
97%
折射率
n20/D 1.459 (lit.)
沸点
242 °C (lit.)
密度
1.18 g/mL at 25 °C (lit.)
官能团
chloro
SMILES字符串
ClC(=O)N1CCCCC1
InChI
1S/C6H10ClNO/c7-6(9)8-4-2-1-3-5-8/h1-5H2
InChI key
BIFDXOOJPDHKJH-UHFFFAOYSA-N
应用
Reactant for synthesis of:
A coumarin-based HIV-1 Vpr inhibitor
Antitumor agents as potent chemosensitizers
Oxime carbamates as reversible inhibitors of fatty acid amide hydrolase
Dipeptidyl peptidase 4 inhibitors for the treatment of type 2 diabetes
Bisarylmaleimide glycogen synthase kinase-3 inhibitors
Lysosomal acid lipase inhibitors and potential Niemann-Pick type C disease therapeutics
A coumarin-based HIV-1 Vpr inhibitor
Antitumor agents as potent chemosensitizers
Oxime carbamates as reversible inhibitors of fatty acid amide hydrolase
Dipeptidyl peptidase 4 inhibitors for the treatment of type 2 diabetes
Bisarylmaleimide glycogen synthase kinase-3 inhibitors
Lysosomal acid lipase inhibitors and potential Niemann-Pick type C disease therapeutics
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Choi H, et al.
Bull. Korean Chem. Soc., 32(11), 3941-3941 (2011)
Self-assembling decacyclene triimides prepared through a regioselective hextuple Friedel-Crafts carbamylation.
Toan V Pho et al.
Angewandte Chemie (International ed. in English), 52(5), 1446-1451 (2012-12-21)
Jure Borišek et al.
Journal of medicinal chemistry, 58(17), 6928-6937 (2015-08-19)
Cathepsin K is a major drug target for osteoporosis and related-bone disorders. Using a combination of virtual combinatorial chemistry, QSAR modeling, and molecular docking studies, a series of cathepsin K inhibitors based on N-(functionalized benzoyl)-homocycloleucyl-glycinonitrile scaffold was developed. In order
New nordihydroguaiaretic acid derivatives as anti-HIV agents.
Hwu JR, et al.
Bioorganic & Medicinal Chemistry Letters, 18(6), 1884-1888 (2008)
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