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7597-56-0

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7597-56-0 Usage

Uses

Ethyl Malonamate can be used for herbicide and herbicide antidote.

Synthesis Reference(s)

Synthetic Communications, 23, p. 3149, 1993 DOI: 10.1080/00397919308011173

Purification Methods

The amide crystallises from Et2O or by slow evaporation of an aqueous solution as colourless crystals [Snyder & Elston J Am Chem Soc 76 3039 1954, McAlvain & Schroeder J Am Chem Soc 71 45 1949, Rising et al. J Biol Chem 89 20 1930]. [Beilstein 2 IV 1887.]

Check Digit Verification of cas no

The CAS Registry Mumber 7597-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7597-56:
(6*7)+(5*5)+(4*9)+(3*7)+(2*5)+(1*6)=140
140 % 10 = 0
So 7597-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO3/c1-2-9-5(8)3-4(6)7/h2-3H2,1H3,(H2,6,7)

7597-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl Carbamoylacetate

1.2 Other means of identification

Product number -
Other names ethyl 3-amino-3-oxopropanoate

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:7597-56-0 SDS

7597-56-0Relevant articles and documents

SYNTHESIS AND TAUTOMERISM OF 1-SUBSTITUTED 3,3-DIALKYL-3,4-DIHYDROISOQUINOLINES

Aleksandrov, B. B.,Gavrilov, M. S.,Vakhrin, M. I.,Shklyaev, V. S.

, p. 662 - 665 (2007/10/02)

A number of ethyl esters of 3,3-dialkyl-3,4-dihydroisoquinoline Δ1(2H),α-α-alkylacetic acids have been synthesized.The effect of replacement of α-hydrogen by alkyl radicals on the azomethine-enamine tautomeric equilibrium was shown.

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