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4,5-Dichloro-2-nitrobenzoic acid is an organic compound characterized by its molecular formula C7H3Cl2NO4. This chemical features a benzoic acid structure with two chlorine atoms at the 4th and 5th positions and a nitro group at the 2nd position. It is a yellow crystalline solid with a melting point of approximately 185°C. 4,5-Dichloro-2-nitrobenzoic acid is primarily used in the synthesis of pharmaceuticals and other organic compounds due to its reactive functional groups, which can participate in various chemical reactions. It is also known for its potential applications in the development of dyes and pigments. However, due to its chemical reactivity and potential health hazards, it is essential to handle 4,5-dichlor0-2-nitrobenzoic acid with proper safety measures and in accordance with established guidelines.

2011-09-8

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2011-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2011-09-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2011-09:
(6*2)+(5*0)+(4*1)+(3*1)+(2*0)+(1*9)=28
28 % 10 = 8
So 2011-09-8 is a valid CAS Registry Number.

2011-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 4,5-Dichlor-2-nitro-benzoesaeure

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:2011-09-8 SDS

2011-09-8Relevant academic research and scientific papers

Identification and optimization of anthranilic sulfonamides as novel, selective cholecystokinin-2 receptor antagonists

Allison, Brett D.,Phuong, Victor K.,McAtee, Laura C.,Rosen, Mark,Morton, Magda,Prendergas, Clodagh,Barrett, Terry,Lagaud, Guy,Freedman, Jamie,Li, Na,Wu, Xiaodong,Venkatesan, Hariharan,Pippel, Marna,Woods, Craig,Rizzolio, Michèle C.,Hack, Michael,Hoey, Kenway,Deng, Xiaohu,King, Christopher,Shankley, Nigel P.,Rabinowitz, Michael H.

, p. 6371 - 6390 (2008/04/18)

A high throughput screening approach to the identification of selective cholecystokinin-2 receptor (CCK-2R) ligands resulted in the discovery of a novel series of antagonists, represented by 1-[2-[(2,1,3-benzothiadiazol-4- ylsulfonyl)amino]-5-chlorobenzoy

Benzo[1,2,5]thiadiazole compounds

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Page 25, (2008/06/13)

Certain amidophenyl-sulfanylamino-benzo[1,2,5]thiadiazole compounds are CCK2 modulators useful in the treatment of CCK2 mediated diseases.

Process for the preparation of fluorinated benzoic acids

-

, (2008/06/13)

A process for the preparation of 2-chloro-4,5-difluorobenzoic acid and 2,4,5-trifluorobenzoic acid as well as synthetic intermediates useful in and prepared according thereto, comprising reacting a nitrobenzene having the formula STR1 wherein X is chloro or fluoro, with an appropriate carbanion to form a compound having the formula STR2 wherein one of Y and Z is chloro and the other is nitro, and R is a radical selected from the group consisting of --CCl3, --CH2 NO2, --CH(NO2)R1, --CH(CO2 R1)2, --CH(C(O)R2)2, --CH(CN)CO2 R1, --CH(CO2 R1)COR2 and --COR2 where R1 is alkyl or arylalkyl and R2 is alkyl, aryl or arylalkyl and, where appearing more than once in such a radical, R1 and R2 may be the same or different at each occurrence.

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