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193264-92-5

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193264-92-5 Usage

Chemical Class

Pyrrole derivatives

Explanation

This compound belongs to the class of pyrrole derivatives, which are organic compounds containing a pyrrole ring.

Explanation

The compound is derived from pyrrole-1,3-dicarboxylic acid by attaching an ester group to the pyrrole ring.
3. Presence of tert-butyl and phenylmethyl groups

Explanation

The compound is characterized by the presence of both a tert-butyl (1,1-dimethylethyl) and a phenylmethyl group, which contribute to its unique chemical properties and reactivity.

Explanation

Due to its unique chemical properties and reactivity, this compound is commonly used as a building block for the synthesis of various drugs and active pharmaceutical ingredients.
5. Use as a reference standard in analytical chemistry

Structure

Ester derivative of pyrrole-1,3-dicarboxylic acid

Application in pharmaceutical industry

Building block for drug synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 193264-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,2,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193264-92:
(8*1)+(7*9)+(6*3)+(5*2)+(4*6)+(3*4)+(2*9)+(1*2)=155
155 % 10 = 5
So 193264-92-5 is a valid CAS Registry Number.

193264-92-5SDS

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 3-benzyl 1-tert-butyl 4,5-dihydro-1H-pyrrole-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names -

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:193264-92-5 SDS

193264-92-5Relevant articles and documents

A convenient route to spiropyrrolidinyl-oxindole alkaloids via C-3 substituted ene-pyrrolidine carbamate radical cyclization

Cossy, Janine,Cases, Manuel,Gomez Pardo, Domingo

, p. 2331 - 2332 (2007/10/03)

A short access to spiropyrrolidinyl-oxindole alkaloids via a substituted ene-pyrrolidine carbamate, synthesized from the commercially available tert- butyl 1-pyrrolidine carboxylate, is described.

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