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2613-33-4

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2613-33-4 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 23, p. 1612, 1958 DOI: 10.1021/jo01105a006

Check Digit Verification of cas no

The CAS Registry Mumber 2613-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2613-33:
(6*2)+(5*6)+(4*1)+(3*3)+(2*3)+(1*3)=64
64 % 10 = 4
So 2613-33-4 is a valid CAS Registry Number.

2613-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-3,5-difluoroaniline

1.2 Other means of identification

Product number -
Other names 4-Chlor-3,5-difluoranilin

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:2613-33-4 SDS

2613-33-4Relevant articles and documents

-

Finger,White

, p. 1612 (1958)

-

SULPHONAMIDES AND COMPOSITIONS THEREOF FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY

-

Page/Page column 473, (2019/05/10)

In one aspect, compounds of Formula AA, or a pharmaceutically acceptable salt thereof, are featured: wherein the variables shown in Formula AA can be as defined anywhere herein. Compounds AA are modulators of NLRP1 and/or NLRP3

Electrophilic aromatic fluorination with fluorine: meta-Directed fluorination of anilines

Alric,Marquet,Billard,Langlois

, p. 661 - 667 (2007/10/03)

Anilines are mainly or selectively fluorinated in the meta-position with F2 when dissolved in triflic acid, sometimes in the presence of small quantities of antimony pentafluoride. The regioselectivity is increased when an electron-donating substituent is present at the para-position.

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