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111468-91-8

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111468-91-8 Usage

General Description

1-[5-(2,2,2-Trichloroacetyl)-1H-pyrrol-3-yl]-1-butanone is a complex chemical compound that belongs to the class of organic compounds known as pyrroles. Pyrroles are compounds that contain a five-membered aromatic ring which consists of one nitrogen atom and four carbon atoms. The mentioned chemical compound has a molecular structure that includes a butanone group, a pyrrol ring, and a trichloroacetic acid residue which contributes to its unique properties. The specific details of its physical characteristics, toxicity, handling precautions, uses, or production methods would likely require a more thorough scientific examination or analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 111468-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,6 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111468-91:
(8*1)+(7*1)+(6*1)+(5*4)+(4*6)+(3*8)+(2*9)+(1*1)=108
108 % 10 = 8
So 111468-91-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10Cl3NO2/c1-2-3-8(15)6-4-7(14-5-6)9(16)10(11,12)13/h4-5,14H,2-3H2,1H3

111468-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[5-(2,2,2-trichloroacetyl)-1H-pyrrol-3-yl]butan-1-one

1.2 Other means of identification

Product number -
Other names trichloroacetylpyrrolylbutanone

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:111468-91-8 SDS

111468-91-8Relevant articles and documents

β-Acylation of ethyl pyrrole-2-carboxylate by Friedel-Crafts acylation: Scope and limitations (synthetic studies on indoles and related compounds. XXXVIII

Tani,Ariyasu,Nishiyama,Hagiwara,Watanabe,Yokoyama,Murakami

, p. 48 - 54 (2007/10/03)

The Friedel-Crafts acylation of ethyl pyrrole-2-carboxylate (3) was studied under several conditions using various Lewis acids and acyl chlorides. The acylation with various acyl chlorides in the presence of aluminum chloride gave exclusively ethyl 4-acylpyrrole-2-carboxylate (5), whereas weaker Lewis acids such as zinc chloride and boron trifluoride etherate gave a mixture of ethyl 4- and 5-acylpyrrole-2-carboxylates.

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