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Key Documents

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D67820

Sigma-Aldrich

2,6-Dichloro-4-nitroaniline

96%

Sinónimos:

Dichloran

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About This Item

Fórmula lineal:
Cl2C6H2(NO2)NH2
Número de CAS:
99-30-9
Peso molecular:
207.01
Beilstein/REAXYS Number:
1459581
EC Number:
202-746-4
MDL number:
MFCD00007677
UNSPSC Code:
12352100
PubChem Substance ID:
24894047
NACRES:
NA.22

assay

96%

form

powder

mp

190-192 °C (lit.)

SMILES string

Nc1c(Cl)cc(cc1Cl)[N+]([O-])=O

InChI

1S/C6H4Cl2N2O2/c7-4-1-3(10(11)12)2-5(8)6(4)9/h1-2H,9H2

InChI key

BIXZHMJUSMUDOQ-UHFFFAOYSA-N

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Categorías relacionadas

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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E Käfer
Mutation research, 241(1), 49-66 (1990-05-01)
Both bleomycin, an antineoplastic drug, and botran (2,6-dichloro-4-nitro-aniline), a fungicide, are known to inhibit growth and induce genetic segregation in diploid tester strains of Aspergillus nidulans when present in agar media. To identify primary effects, samples of induced apparent crossover
Acute toxicity of cadmium, copper, zinc, ammonia, 3,3'-dichlorobenzidine, 2,6-dichloro-4-nitroaniline, methylene chloride, and 2,4,6-trichlorophenol to juvenile grass shrimp and killifish.
D T Burton et al.
Bulletin of environmental contamination and toxicology, 44(5), 776-783 (1990-05-01)
L A Myers et al.
Toxicology and applied pharmacology, 95(1), 139-152 (1988-08-01)
The metabolism of 2,6-dichloro-4-nitroaniline (DCNA) to a unique denitrosated product, 3,5-dichloro-p-aminophenol (DCAP), was investigated in rat hepatic microsomes using an HPLC system containing a reverse-phase column and an electrochemical detector. The parent compound appears to induce its own metabolism. The
Ryota Uehara et al.
Cell motility and the cytoskeleton, 65(2), 100-115 (2007-10-31)
Phosphorylation of myosin regulatory light chain (RLC) at Ser19 (mono-phosphorylation) promotes filament assembly and enhances actin-activated ATPase activity of non-muscle myosin, while phosphorylation at both Ser19 and Thr18 (di-phosphorylation) further enhances the ATPase activity. However, it has not well been
Danielle Palma de Oliveira et al.
Environmental toxicology and chemistry, 28(9), 1881-1884 (2009-05-05)
2,6-Dichloro-4-nitroaniline (dicloran) is a mutagenic aromatic amine used as an agricultural fungicide and in the synthesis of disperse dyes. It is a known mutagen (Salmonella/microsome assay) in strains TA98 and TA100. Dicloran was initially detected, but not quantified, in the
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