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About This Item
Linear Formula:
ClCO2CH2C6H2(OCH3)2NO2
CAS Number:
Molecular Weight:
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
Reagent for introducing the photo-cleavable amino-protecting group NVOC, selectively and very mildly cleaved with 350 nm light
This product has been replaced by 420069-ALDRICH | 4,5-Dimethoxy-2-nitrobenzyl chloroformate 97%
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
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
Regulatory Information
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R.T. Cummings et al.
Tetrahedron Letters, 29, 65-65 (1988)
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
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
S.A. Robertson et al.
Journal of the American Chemical Society, 113, 2722-2722 (1991)
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