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32683-02-6

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32683-02-6 Usage

General Description

ETHYL 2-AMINO-2-CYANOACETATE OXALATE H2O is a chemical compound that is a derivative of the amino acid glycine. It is commonly used as a reagent in organic synthesis and as a building block for the preparation of various pharmaceutical and biologically active compounds. ETHYL 2-AMINO-2-CYANOACETATE OXALATE H2O is a white crystalline solid that is soluble in water, and it has a wide range of applications in the pharmaceutical, chemical, and agrochemical industries. It is also used as a key intermediate in the synthesis of various drugs and other organic compounds. Overall, ETHYL 2-AMINO-2-CYANOACETATE OXALATE H2O is an important compound with diverse applications in the field of organic synthesis and pharmaceutical chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 32683-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,6,8 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32683-02:
(7*3)+(6*2)+(5*6)+(4*8)+(3*3)+(2*0)+(1*2)=106
106 % 10 = 6
So 32683-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2O2/c1-2-9-5(8)4(7)3-6/h4H,2,7H2,1H3

32683-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 2-AMINO-2-CYANOACETATE OXALATE H2O

1.2 Other means of identification

Product number -
Other names ethyl aminocyanoacetate

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:32683-02-6 SDS

32683-02-6Relevant articles and documents

On the Polarographic Reduction Mechanism of Some Heterocyclic Compounds

Malik, Wahid U.,Jain, Rajeev

, p. 191 - 194 (2007/10/02)

For evaluating the mechanistic steps, position at d.m.e. and assigning inner or outer sphere path of electrode processes of a number of pyrazole derivatives, thiazoles and their precursors experiments were carried out in the absence and presence of surfactants.All the compounds gave diffusion-controlled, irreversible waves over the entire pH range (2.0-11.0) studied.In presence of surfactants also, diffusion-controlled but more irreversible waves were obtained.In absence and presence of surfactant (CTAB) values of Kapp and αapp for all these compounds were calculated and have been taken as a proof of inner sphere or outer sphere path of the electrode reaction.Results have been explained on the basis of formation of phenylazo-functionalised surfactant as an intermediate species.

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