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36556-52-2

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36556-52-2 Usage

General Description

2,3-Dichloro-4-fluoroaniline is a chemical compound with the molecular formula C6H4Cl2FN. It is a derivative of aniline, containing two chlorine atoms and one fluorine atom attached to the benzene ring. 2,3-Dichloro-4-fluoroaniline is used in the synthesis of pharmaceuticals and agrochemicals. It is also utilized as an intermediate for the production of dyes, pigments, and other organic compounds. 2,3-Dichloro-4-fluoroaniline is a hazardous chemical and should be handled with care, as it can cause skin and eye irritation, and may be harmful if ingested or inhaled. Safety precautions should be followed when working with this chemical, such as using proper personal protective equipment and working in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 36556-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,5 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36556-52:
(7*3)+(6*6)+(5*5)+(4*5)+(3*6)+(2*5)+(1*2)=132
132 % 10 = 2
So 36556-52-2 is a valid CAS Registry Number.

36556-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Dichloro-4-fluoroaniline

1.2 Other means of identification

Product number -
Other names 2,3,5-TRIFLUORO NITROBENZENE

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:36556-52-2 SDS

36556-52-2Relevant articles and documents

Structure-activity relationship studies on a series of novel, substituted 1-benzyl-5-phenyltetrazole P2X7 antagonists

Nelson, Derek W.,Gregg, Robert J.,Kort, Michael E.,Perez-Medrano, Arturo,Voight, Eric A.,Wang, Ying,Grayson, George,Namovic, Marian T.,Donnelly-Roberts, Diana L.,Niforatos, Wende,Honore, Prisca,Jarvis, Michael F.,Faltynek, Connie R.,Carroll, William A.

, p. 3659 - 3666 (2007/10/03)

1-Benzyl-5-aryltetrazoles were discovered to be novel antagonists for the P2X? receptor. Structure-activity relationship (SAR) studies were conducted around both the benzyl and phenyl moieties. In addition, the importance of the regiochemical substitution

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