C38907
4-氯-3,5-二硝基苯甲酸
97%
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线性分子式:
ClC6H2(NO2)2CO2H
化学文摘社编号:
分子量:
246.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-290-1
Beilstein/REAXYS Number:
668253
MDL number:
产品名称
4-氯-3,5-二硝基苯甲酸, 97%
InChI key
PCTFIHOVQYYAMH-UHFFFAOYSA-N
InChI
1S/C7H3ClN2O6/c8-6-4(9(13)14)1-3(7(11)12)2-5(6)10(15)16/h1-2H,(H,11,12)
SMILES string
OC(=O)c1cc(c(Cl)c(c1)[N+]([O-])=O)[N+]([O-])=O
assay
97%
form
crystals
mp
159-162 °C (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
4.1A - Other explosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
L S Chang et al.
Biochemistry and molecular biology international, 33(6), 1207-1213 (1994-08-01)
Phospholipase A2 (PLA2) from Naja naja atra snake venom was modified with 4-chloro-3,5-dinitrobenzoate, and one major carboxydinitrophenylated (CDNP) PLA2 was separated by high performance liquid chromato-graphy. CDNP-PLA2 contained only one CDNP group on Lys-6 and showed a 93% drop in
A A Jacobs et al.
Biochimica et biophysica acta, 872(1-2), 92-97 (1986-07-25)
Modification of lysine residues with 4-chloro-3,5-dinitrobenzoate results in the loss of the binding capacity of K99 fibrillae to horse erythrocytes (Jacobs, A.A.C., van Mechelen, J.R. and de Graaf, F.K. (1985) Biochim. Biophys. Acta 832, 148-155). In the present study we
J Thiele et al.
Applied and environmental microbiology, 54(5), 1199-1202 (1988-05-01)
4-Chlorobenzoate dehalogenase from Pseudomonas sp. strain CBS3 converted 4-chloro-3,5-dinitrobenzoate to 3,5-dinitro-4-hydroxybenzoate and 1-chloro-2,4-dinitrobenzene to 2,4-dinitrophenol. The activities were 0.13 mU/mg of protein for 4-chloro-3,5-dinitrobenzoate and 0.16 mU/mg of protein for 1-chloro-2,4-dinitrobenzene compared with 0.5 mU/mg of protein for 4-chlorobenzoate.
E L Gross et al.
Biochimica et biophysica acta, 1016(1), 107-114 (1990-03-15)
Chemical modification of plastocyanin was carried out using 4-chloro-3,5-dinitrobenzoic acid, which has the effect of replacing positive charges on amino groups with negatively charged carboxyl groups. Four singly-modified forms were obtained which were separated using anion exchange FPLC. The four
H Greim et al.
Advances in experimental medicine and biology, 136 Pt B, 1389-1398 (1981-01-01)
Metabolic inactivation of chemicals may prevent toxic effects of reactive intermediates when present at low levels whereas inactivation may be overcome at high levels changing dose-effect relation. This is demonstrated in various in vitro test systems: a) Monooxygenase-mediated metabolism causes
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