222054
4-正庚基苯甲酰氯
99%
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关于此项目
线性分子式:
CH3(CH2)6C6H4COCl
化学文摘社编号:
分子量:
238.75
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
256-648-1
MDL number:
产品名称
4-正庚基苯甲酰氯, 99%
InChI key
WHTFLTOKFXTJGV-UHFFFAOYSA-N
InChI
1S/C14H19ClO/c1-2-3-4-5-6-7-12-8-10-13(11-9-12)14(15)16/h8-11H,2-7H2,1H3
SMILES string
CCCCCCCc1ccc(cc1)C(Cl)=O
assay
99%
form
liquid
refractive index
n20/D 1.5218 (lit.)
density
1.002 g/mL at 25 °C (lit.)
functional group
acyl chloride
Quality Level
Application
4-Heptylbenzoyl chloride was used in the synthesis of 3-O-acyl derivative by reacting with betulinic acid.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Rama Mukherjee et al.
Bioorganic & medicinal chemistry letters, 14(12), 3169-3172 (2004-05-20)
New 3-O-acyl, 3-benzylidene, 3-hydrazone, 3-hydrazine, 17-carboxyacryloyl ester derivatives of betulinic acid (2-6, 8-11, 13, 17, 18, 21, and 22) were synthesized and evaluated in vitro for anti-angiogenic activity on endothelial cell cytotoxicity, specificity, and tube-formation ability. All derivatives reported here
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