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1H-Pyrazolo[4,3-c]pyridine-6-carboxylic acid, 1-phenyl-4-(phenylamino)-, ethyl ester is a chemical compound with the molecular formula C23H19N3O2. It is an ethyl ester derivative of 1-phenyl-4-(phenylamino)-1H-pyrazolo[4,3-c]pyridine-6-carboxylic acid. 1H-Pyrazolo[4,3-c]pyridine-6-carboxylic acid, 1-phenyl-4-(phenylamino)-, ethyl ester features a pyrazole ring, a pyridine ring, and two phenyl groups, making it a versatile molecule for designing new drugs and pharmaceuticals.

137368-76-4

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137368-76-4 Usage

Uses

Used in Organic Synthesis:
1H-Pyrazolo[4,3-c]pyridine-6-carboxylic acid, 1-phenyl-4-(phenylamino)-, ethyl ester is used as a building block in organic synthesis for the creation of novel heterocyclic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1H-Pyrazolo[4,3-c]pyridine-6-carboxylic acid, 1-phenyl-4-(phenylamino)-, ethyl ester serves as a key intermediate in the synthesis of potential biologically active molecules, contributing to the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 137368-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,3,6 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 137368-76:
(8*1)+(7*3)+(6*7)+(5*3)+(4*6)+(3*8)+(2*7)+(1*6)=154
154 % 10 = 4
So 137368-76-4 is a valid CAS Registry Number.

137368-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylamino-6-ethoxycarbonyl-1-phenyl-1H-pyrazolo<4,3-c>pyridine

1.2 Other means of identification

Product number -
Other names 1-Phenyl-4-phenylamino-1H-pyrazolo[4,3-c]pyridine-6-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:137368-76-4 SDS

137368-76-4Downstream Products

137368-76-4Relevant academic research and scientific papers

Pyrido annelation reaction by a tandem aza Wittig/electrocyclic ring-closure strategy: Preparation of pyrazolo[4,3-c]- and pyrazolo[3,4-c]pyridine derivatives

Molina,Aller,Lorenzo

, p. 6737 - 6746 (2007/10/02)

The aza Wittig-type reaction of iminophosphorane 3, prepared from 5-formyl-1-phenylpyrazole by sequential treatment with ethyl azidoacetate and triphenylphosphine, with isocyanates, ketenes, aldehydes and carbon disulfide leads to the functionalized pyrazolo[4,3-c]pyridines 5, 7, 9 and 11 respectively. Iminophosphorane 15, prepared from 4-formyl-1-phenylpyrazole, undergoes pyrido annelation by reaction with ketenes to give the isomeric pyrazolo[3,4-c]pyridines 22 in modest yields.

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