23245
4,5-二甲氧基-2-硝基苄基氯甲酸酯
purum, ≥97.0% (AT)
别名:
6-硝基藜芦基氯甲酸酯, 6-硝基藜芦氯甲酸, NVOC 氯化物, NVOC-Cl
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关于此项目
线性分子式:
ClCO2CH2C6H2(OCH3)2NO2
化学文摘社编号:
分子量:
275.64
PubChem Substance ID:
UNSPSC Code:
12352000
Beilstein/REAXYS Number:
2389168
MDL number:
grade
purum
assay
≥97.0% (AT)
mp
125 °C (dec.) (lit.)
storage temp.
2-8°C
SMILES string
COc1cc(COC(Cl)=O)c(cc1OC)[N+]([O-])=O
InChI
1S/C10H10ClNO6/c1-16-8-3-6(5-18-10(11)13)7(12(14)15)4-9(8)17-2/h3-4H,5H2,1-2H3
InChI key
RWWPKIOWBQFXEE-UHFFFAOYSA-N
Other Notes
用于引入光裂解胺基保护基团 NVOC 的试剂，NVOC 在 350nm 光下极其温和地选择性裂解
This product has been replaced by 420069-ALDRICH | 4,5-Dimethoxy-2-nitrobenzyl chloroformate 97%
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
S P Fodor et al.
Science (New York, N.Y.), 251(4995), 767-773 (1991-02-15)
Solid-phase chemistry, photolabile protecting groups, and photolithography have been combined to achieve light-directed, spatially addressable parallel chemical synthesis to yield a highly diverse set of chemical products. Binary masking, one of many possible combinatorial synthesis strategies, yields 2n compounds in
R.T. Cummings et al.
Tetrahedron Letters, 29, 65-65 (1988)
S.A. Robertson et al.
Journal of the American Chemical Society, 113, 2722-2722 (1991)
V.N.R. Pillai
Synthesis, 1-1 (1980)
G Marriott
Biochemistry, 33(31), 9092-9097 (1994-08-09)
A simple method is described to prepare caged (inactive) protein complexes using the amino group-directed photo-deprotection group [(nitroveratryl)oxy]chlorocarbamate (NVOC-Cl). In this study, I show how the polymerization activity of G-actin in physiological salt solution is lost upon conjugation of essential
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