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Ethyl (2Z)-2-cyano-3-[(methylcarbamoyl)amino]prop-2-enoate is a complex organic compound with the chemical formula C9H12N3O3. It is a derivative of acrylic acid, featuring a cyano group (-CN) and an amino group (-NH2) attached to the propenoate chain. The molecule also contains a methylcarbamoyl group (-NHCOCH3), which is a carbamate functional group. ethyl (2Z)-2-cyano-3-[(methylcarbamoyl)amino]prop-2-enoate is characterized by its conjugated double bond system (2Z), which contributes to its chemical reactivity and potential applications in the synthesis of various pharmaceuticals and agrochemicals. Its structure and properties make it a versatile intermediate in organic synthesis, particularly in the preparation of compounds with potential biological activity.

5327-29-7

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5327-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5327-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5327-29:
(6*5)+(5*3)+(4*2)+(3*7)+(2*2)+(1*9)=87
87 % 10 = 7
So 5327-29-7 is a valid CAS Registry Number.

5327-29-7SDS

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 2-cyano-3-(methylcarbamoylamino)prop-2-enoate

1.2 Other means of identification

Product number -
Other names ethyl 2-cyano-3-[(methylcarbamoyl)amino]prop-2-enoate

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5327-29-7 SDS

5327-29-7Downstream Products

5327-29-7Relevant academic research and scientific papers

Syntheses with Nitriles, XCV: Deamination of Cytosine Derivatives

Deshmukh, M.,Mittelbach, M.,Junek, H.

, p. 91 - 98 (2007/10/02)

Treatment of 2-formyl-3-dimethylamino-propenenitrile (1a) and 2-ethoxycarbonyl-3-dimethylamino-propenenitrile (1b), resp., with substituted ureas led to the 2-cyano-3-ureidoacrylates 2, which can be cyclized under alkaline conditions to give 5-formyl-5-cy

CYCLIZATION DICHOTOMY OF ESTERS OF 3-UREIDO-2-CYANO-2-PROPENOIC AND 3-UREIDO-2-ACYL-2-PROPENOIC ACIDS

Ledvina, Miroslav,Farkas, Jiri

, p. 1841 - 1852 (2007/10/02)

The preparation of E and Z isomers of 3-ureido-2-cyano-2-propenoates Ia-Id and their base-catalyzed isomerization and cyclization to 5-carboxycytosine derivatives IIa-IIf and 5-cyanouracil derivatives IIIa and IIIb is described.Also described is the preparation of 3-ureido-2-acyl-2-propenoates Va-Vd and their base-catalyzed cyclization to 5-carboxy-2(1H)-pyrimidone derivatives VIa-VIc and 5-acyluracils VIIa-VIIc.

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