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69624-11-9

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69624-11-9 Usage

Uses

3-Chloro-1H-pyrrole is a useful reactant and reagent for organic reactions and synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 69624-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69624-11:
(7*6)+(6*9)+(5*6)+(4*2)+(3*4)+(2*1)+(1*1)=149
149 % 10 = 9
So 69624-11-9 is a valid CAS Registry Number.

69624-11-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-1H-pyrrole

1.2 Other means of identification

Product number -
Other names 3-chloropyrrole

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:69624-11-9 SDS

69624-11-9Relevant articles and documents

MALT1 INHIBITORS AND USES THEREOF

-

Page/Page column 51-52, (2021/10/15)

The invention provides compounds of formula (I) wherein R1, R2, R3, R4 and R5 are as defined in the specification which are potent inhibitors of the enzyme MALT1 and are useful in the treatment of autoimmune disorders and diseases and as an immunooncology approach to the treatment of cancer, especially bladder cancer, colon cancer, hepatocellular cancer and small cell or non-small cell lung cancer.

Acid Catalyzed Chlorination of Pyrrole With N-Chloroacetanilide

Rosa, Michael De

, p. 1585 (2007/10/02)

The chlorination of pyrrole with N-chloroacetanilide was catalyzed by acetic acid.Transfer of Cl+ occurred directly to the α and β positions of pyrrole and a mixture of 2-chloro-, 3-chloro- and 2,5-dichloropyrrole was formed.The α/β ratio was 10:1 under competitive conditions.

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