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1H-Pyrrole-1-carboxylic acid, 4-formyl-2,3-dihydro-, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82483-66-7

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82483-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82483-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82483-66:
(7*8)+(6*2)+(5*4)+(4*8)+(3*3)+(2*6)+(1*6)=147
147 % 10 = 7
So 82483-66-7 is a valid CAS Registry Number.

82483-66-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-formyl-2,3-dihydro-1H-pyrrole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Formyl-2,3-dihydro-pyrrole-1-carboxylic acid methyl 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:82483-66-7 SDS

82483-66-7Downstream Products

82483-66-7Relevant academic research and scientific papers

Electroorganic Chemistry. 60. Electroorganic Synthesis of Enamides and Enecarbamates and Their Utilization in Organic Synthesis.

Shono, Tatsuya,Matsumura, Yoshihiro,Tsubata, Kenji,Sugihara, Yoshihiro,Yamane, Shin-ichiro,et. al.

, p. 6697 - 6703 (2007/10/02)

A variety of enecarbamates and enamides were synthesized from α-methoxy carbamates and α-methoxy amides prepared by anodic methoxylation of amine derivatives.Some new carbon-carbon bond-forming reactions and hydroxylation at the β position of amines have been accomplished by using these enecarbamates and enamides as key intermediates.Also, new synthetic routes of nicotinaldehyde and pyrrole derivatives have been exploited by utilizing anodic dimethoxylation of carbamates of piperidine and pyrrolidine, respectively.

A NEW METHOD OF ACYLATION AT β-POSITION OF ALIPHATIC AMINES

Shono, Tatsuya,Matsumura, Yoshihiro,Tsubata, Kenji,Sugihara, Yoshihiro

, p. 1201 - 1204 (2007/10/02)

A new method to introduce an acyl or a formyl group to β-position of aliphatic amines was studied using encarbamates, prepared from α-methoxycarbamates, as key intermediates.

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