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2-Chloro-3,5-dinitrobenzamide is a chemical compound with the molecular formula C7H4ClN3O5. It is a derivative of benzamide, featuring a chlorine atom at the 2nd position, and nitro groups at the 3rd and 5th positions on the benzene ring. 2-chloro-3,5-dinitrobenzamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its reactive functional groups. It is also used as an intermediate in the preparation of dyes and other organic compounds. The compound is characterized by its yellow crystalline appearance and is sensitive to light, which can lead to decomposition. It is important to handle this chemical with care, as it may have toxic properties and should be stored away from light and heat to maintain its stability.

6266-51-9

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6266-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6266-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6266-51:
(6*6)+(5*2)+(4*6)+(3*6)+(2*5)+(1*1)=99
99 % 10 = 9
So 6266-51-9 is a valid CAS Registry Number.

6266-51-9SDS

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-chloro-3,5-dinitrobenzamide

1.2 Other means of identification

Product number -
Other names 2-chloro-3,5-dinitro-benzamide

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:6266-51-9 SDS

6266-51-9Relevant academic research and scientific papers

Hypoxia-selective antitumor agents. 14. Synthesis and hypoxic cell cytotoxicity of regioisomers of the hypoxia-selective cytotoxin 5-[N,N- bis(2-chloroethyl)amino]-2,4-dinitrobenzamide

Palmer,Wilson,Anderson,Boyd,Denny

, p. 2518 - 2528 (2007/10/03)

A series of regioisomers of the novel hypoxia-selective cytotoxin (HSC) 5- [N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (2a) have been prepared by displacement of the chloro group from methyl chlorodinitrobenzoates or the corresponding carboxamides

Synthesis and Spectral Characterization of Blue Dyes of the Benzene Series

Thiel, W.,Mayer, R.,Jauer, E.-A.,Modrow, H.,Dost, H.

, p. 497 - 514 (2007/10/02)

53 Donor-acceptor substituted azo dyes of the benzene series were prepared by diazonium-coupling reactions (1a-s) or halogen-cyanide exchange (->2a-x, 3a-j).Described are the preparation of the amines 4a-m and the coupling compounds 5a-t and the procedure of diazotizing and coupling.The colouristic and spectroscopic data show that compounds of the general formula 1 are excellent brilliant blue azo dyes usefull for dyeing polyester material.

Cyano phenylene dioxamic molecules

-

, (2008/06/13)

Compounds represented below SPC1 And pharmaceutical compositions thereof, the compositions including the non-substituted phenylene dioxamates are useful in the prophylactic treatment of sensitized mammals for allergy and all anaphylactic reactions of a reagin or non-reagin mediated nature.

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