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线性分子式:
ClCO2CH2C6H4NO2
化学文摘社编号:
分子量:
215.59
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
EC Number:
224-708-6
MDL number:
Beilstein/REAXYS Number:
912446
产品名称
对硝基氯甲酸苄酯, 97%
InChI key
MHSGOABISYIYKP-UHFFFAOYSA-N
InChI
1S/C8H6ClNO4/c9-8(11)14-5-6-1-3-7(4-2-6)10(12)13/h1-4H,5H2
SMILES string
[O-][N+](=O)c1ccc(COC(Cl)=O)cc1
assay
97%
reaction suitability
reaction type: Carbonylations
mp
32-34 °C (lit.)
application(s)
peptide synthesis
functional group
chloro
nitro
storage temp.
2-8°C
Quality Level
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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
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Eun Hyang Jang et al.
International journal of pharmaceutics, 580, 119237-119237 (2020-03-24)
Hypoxia is a characteristic feature of various ischemic diseases, including cancer. This study describes the development of glycol chitosan nanoparticles, hydrophobically modified with 4-nitrobenzyl chloroformate and folic acid (FA), that can specifically release drugs under hypoxic conditions. This hypoxia-responsive glycol
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