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1,3(2H)-Pyridazinedicarboxylic acid, tetrahydro-, 3-methyl 1-(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79024-87-6

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79024-87-6 Usage

Type of compound

Organic compound

Derivative of

Pyridazine

Common uses

Production of pharmaceuticals and agrochemicals

Potential applications

Intermediate in the synthesis of a wide range of organic compounds

Biological activities

Shown promising results in various studies

Safety precautions

Handle and use with caution, may have hazardous properties

Professional guidance

Should be used only under the direction of trained professionals

Appropriate settings

Appropriate laboratory settings required for handling and use

Structural features

Contains a pyridazine ring, a tetrahydro group, a 3-methyl group, and a phenylmethyl ester group.

Check Digit Verification of cas no

The CAS Registry Mumber 79024-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,2 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79024-87:
(7*7)+(6*9)+(5*0)+(4*2)+(3*4)+(2*8)+(1*7)=146
146 % 10 = 6
So 79024-87-6 is a valid CAS Registry Number.

79024-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-benzyloxycarbonylhexahydropyridazine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1-benzyl 3-methyl piperazine-1,3-dicarboxylate

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:79024-87-6 SDS

79024-87-6Upstream product

79024-87-6Relevant academic research and scientific papers

Synthesis of cyclic α-hydrazino acids

Duttagupta, Indranil,Goswami, Koushik,Sinha, Surajit

, p. 8347 - 8357 (2012)

Synthesis of five-, six-, seven-, eight-, and nine-membered cyclic α-hydrazino acids from a common starting material 'diethylmalonate' with 26, 16, 34, 13.5, and 13.33% overall yields is described. Sequential allylation or homoallylation and electrophilic amination followed by cyclization gave the desired rings. The methyl esters of eight- and nine-membered rings were synthesized by RCM and the corresponding free acids were generated after hydrolysis in the presence of 1 M BBr3 solution in DCM.

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