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ETHYL-1-BENZYL-2,4-DIMETHYLPYRROLE-3-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92977-40-7

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92977-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92977-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,7 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92977-40:
(7*9)+(6*2)+(5*9)+(4*7)+(3*7)+(2*4)+(1*0)=177
177 % 10 = 7
So 92977-40-7 is a valid CAS Registry Number.

92977-40-7SDS

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 1-benzyl-5-ethyl-2,4-dimethylpyrrole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1-benzyl-2,4-dimethyl-pyrrole-3-carboxylic acid ethyl ester

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:92977-40-7 SDS

92977-40-7Relevant academic research and scientific papers

Silver-catalyzed chemoselective annulation of propargyl amines with alkynes for access to pyridines and pyrroles

Nizami, Tauqir A.,Hua, Ruimao

, p. 6080 - 6084 (2017/09/23)

The annulation of propargyl amines with electron-deficient alkynes in the presence of silver salts affording pyridines and pyrroles has been developed. The chemoselective [4+2] or [3+2] annulation approach to pyridines or pyrroles depends on the structure

Synthesis of 1,2,3,5-tetrasubstituted pyrrole derivatives from 2-(2-bromoallyl)-1,3-dicarbonyl compounds

Demir, Ayhan S,Akhmedov, Idris M,Sesenoglu, ?zge

, p. 9793 - 9799 (2007/10/03)

2-(2-Bromoallyl)-1,3-dicarbonyl compounds are converted into β-enamino, β-hydrazino esters and ketones, followed by base-promoted cyclization, leading to the formation of the corresponding 1,2,3,5-tetrasubstituted pyrroles. 1,2,4- and 1,2,3,4-Substituted pyrroles are also isolated as minor products. Starting from the 2-(2-bromoallyl)-cyclohexane-1,3-dione the corresponding tetrahydro indolone is prepared in good yield.

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