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Tetrahydro-1,3(2H)-pyridazinedicarboxylic acid 1-(phenylmethyl) ester is a complex chemical compound that belongs to the pyridazines class of chemicals. It is characterized by a six-membered ring with two nitrogen atoms, a carboxylic acid ester, and the introduction of a phenylmethyl group. The carboxylic acid ester is formed by replacing the hydrogen of an acid with an alkyl or other organic group, which in this case is phenylmethyl. The combination of these components gives Tetrahydro-1,3(2H)-pyridazinedicarboxylic acid 1-(phenylmethyl) ester its unique chemical properties.

72120-54-8

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72120-54-8 Usage

Uses

Used in Pharmaceutical Industry:
Tetrahydro-1,3(2H)-pyridazinedicarboxylic acid 1-(phenylmethyl) ester is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique chemical structure allows for the development of new compounds with potential therapeutic applications.
Used in Chemical Research:
Tetrahydro-1,3(2H)-pyridazinedicarboxylic acid 1-(phenylmethyl) ester is used as a research compound in the field of organic chemistry. Its complex structure provides opportunities for studying the properties and reactions of pyridazines and carboxylic acid esters, contributing to the advancement of chemical knowledge.
Used in Material Science:
Tetrahydro-1,3(2H)-pyridazinedicarboxylic acid 1-(phenylmethyl) ester is used as a building block in the development of new materials. Its unique chemical properties can be exploited to create novel materials with specific characteristics, such as improved stability or reactivity, for various applications in material science.

Check Digit Verification of cas no

The CAS Registry Mumber 72120-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,2 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72120-54:
(7*7)+(6*2)+(5*1)+(4*2)+(3*0)+(2*5)+(1*4)=88
88 % 10 = 8
So 72120-54-8 is a valid CAS Registry Number.

72120-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-((Benzyloxy)carbonyl)hexahydropyridazine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-phenylmethoxycarbonyldiazinane-3-carboxylic acid

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:72120-54-8 SDS

72120-54-8Relevant academic research and scientific papers

Piperazic acid derivatives inhibit Gli1 in Hedgehog signaling pathway

Khatra, Harleen,Kundu, Jayanta,Khan, Pragya Paramita,Duttagupta, Indranil,Pattanayak, Sankha,Sinha, Surajit

, p. 4423 - 4426 (2016)

Piperazic acid, a non-proteinogenic amino acid, found in complex secondary metabolites and peptide natural substances, has shown down regulation of Gli1 expression in Hedgehog signaling pathway in cell based assays. Further structure activity relationship

IMPROVED PROCESS FOR THE MANUFACTURE OF 1,2-DISUBSTITUTED HEXAHYDROPYRIDAZINE-3-CARBOXYLIC ACIDS AND ESTERS THEREOF

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Page/Page column 13-14, (2010/02/11)

The invention relates to an improved process for the manufacture of 1,2-disubstituted hexahydro-pyridazine-3-carboxylic acids and esters thereof by reacting N,N’-disubstituted hydrazine with 2,5-dihalogenated valeric acids and thereof by means of phase transfer catalysis. Said pyridazine carboxylic acids and esters thereof can be used as intermediates for the production of pharmaceutical products

Process for preparing hexahydropyridazine-3-carboxylic acid derivatives

-

Page 3, (2008/06/13)

According to the process of the invention, the hexahydropyridazine-3-carboxylic acid derivatives are prepared by reacting a compound of formula (II) with a compound of formula (III) in the presence of a base with a pK of greater than or equal to 8.5, in a ketone organic solvent, to obtain an intermediate compound that is not isolated and that is treated with a basic aqueous medium. By means of this process, the derivatives are obtained more quickly and more economically.

PREPARATION OF 1-(BENZYLOXYCARBONYL)HEXAHYDRO-3-PYRIDAZINE CARBOXYLIC ACID, A PROTECTED PIPERAZIC ACID

Adams, C. E.,Aguilar, D.,Hertel, S.,Knight, W. H.,Paterson, J.

, p. 2225 - 2232 (2007/10/02)

A preparation of 1-(benzyloxycarbonyl)hexahydro-3-pyridazinecarboxylic acid in five steps (73percent overall yield) from 4-phenylurazole is described.

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