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105370-80-7

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105370-80-7 Usage

General Description

(R)-pyrrolidine-1,2-dicarboxylic acid 1-phenyl ester is a chemical compound with the molecular formula C13H15NO4. It is an ester derivative of the amino acid pyroglutamic acid, also known as 5-oxoproline. (R)-pyrrolidine-1,2-dicarboxylic acid 1-phenyl ester has been studied for its potential pharmaceutical applications, particularly in the treatment of neurodegenerative diseases and cognitive impairments. It is believed to have neuroprotective and cognitive-enhancing properties, making it a potential candidate for drug development in the fields of neurology and psychiatry. Additionally, (R)-pyrrolidine-1,2-dicarboxylic acid 1-phenyl ester may also have applications in the synthesis of other pharmaceutical compounds and in academic research.

Check Digit Verification of cas no

The CAS Registry Mumber 105370-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,7 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105370-80:
(8*1)+(7*0)+(6*5)+(5*3)+(4*7)+(3*0)+(2*8)+(1*0)=97
97 % 10 = 7
So 105370-80-7 is a valid CAS Registry Number.

105370-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-pyrrolidine-1,2-dicarboxylic acid 1-phenyl ester

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

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More Details:105370-80-7 SDS

105370-80-7Relevant articles and documents

PROCESS FOR THE PREPARATION OF 5-SUBSTSITUTED INDOLE DERIVATIVE

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Page/Page column 28, (2012/02/01)

The present invention relates to an improved and industrially advantageous process for preparation of eletri tan of formula I,or pharmaceutically acceptable salts thereof from bromo indole intermediate of formula II, through isolation of N-acetylated bromo indole intermediate of formula III, to elude carrying forward of impurities to next stage. The present invention relates to process for the preparation of 5-bromo-3-[(R)-l-methyl-pyrrolidin-2- lmeth l -lH-indol of formula II, a key intermediate for the synthesis of eletriptan or pharmaceutically acceptable salts thereof, through novel keto carbamate intermediate. The present invention also relates to novel process for the preparation of a-form of eletriptan hydrobromide.

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