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19861-62-2

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19861-62-2 Usage

General Description

2,4-Dichloro-5-nitrobenzoic acid is a synthetic chemical compound that is commonly used as a herbicide and plant growth regulator. It belongs to the class of benzoic acids, which are known for their herbicidal properties. The compound is a white crystalline solid with a molecular formula of C7H3Cl2NO4 and a molecular weight of 235.01 g/mol. It is soluble in organic solvents and slightly soluble in water. 2,4-Dichloro-5-nitrobenzoic acid works by disrupting the normal growth processes in plants, leading to inhibited cell division and ultimately causing the plant to die. Due to its herbicidal properties, it is important to handle this chemical with care and follow proper safety precautions when using it.

Check Digit Verification of cas no

The CAS Registry Mumber 19861-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,6 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19861-62:
(7*1)+(6*9)+(5*8)+(4*6)+(3*1)+(2*6)+(1*2)=142
142 % 10 = 2
So 19861-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl2NO4/c8-4-2-5(9)6(10(13)14)1-3(4)7(11)12/h1-2H,(H,11,12)

19861-62-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dichloro-5-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 4,6-Dichloro-3-nitrobenzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19861-62-2 SDS

19861-62-2Relevant articles and documents

Optimization of 2,4-diarylanilines as non-nucleoside HIV-1 reverse transcriptase inhibitors

Sun, Lian-Qi,Qin, Bingjie,Huang, Li,Qian, Keduo,Chen, Chin-Ho,Lee, Kuo-Hsiung,Xie, Lan

scheme or table, p. 2376 - 2379 (2012/05/05)

The current optimization of 2,4-diarylaniline analogs (DAANs) on the central phenyl ring provided a series of new active DAAN derivatives 9a-9e, indicating an accessible modification approach that could improve anti-HIV potency against wild-type and resis

QUINAZOLINONE COMPOUNDS

-

Page/Page column 29-30, (2010/07/09)

The present invention relates to quinazolinone compounds, processes for their preparation and their use as pharmaceutical agents for the treatment of Parkinson's disease (PD). The quinazolinone compounds are of general formula (I).

Process for the production of nitro derivatives of aromatic compounds

-

, (2008/06/13)

Nitroderivates of aromatic compounds which are difficult to nitrate, can readily be obtained by nitration providing that the aromatic compound is treated with nitric acid or another nitrating agent in the presence of aliphatic or cycloaliphatic hydrocarbons monosubstituted or polysubstituted by halogen, the nitro group or an alkyl sulphonyl group, and the nitro derivative formed subsequently isolated.

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