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62981-80-0

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62981-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62981-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,8 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62981-80:
(7*6)+(6*2)+(5*9)+(4*8)+(3*1)+(2*8)+(1*0)=150
150 % 10 = 0
So 62981-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO3/c1-3-12-8(11)7(5-9)4-6(2)10/h7H,3-4H2,1-2H3

62981-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-cyano-4-oxopentanoate

1.2 Other means of identification

Product number -
Other names 2-cyano-4-oxopentanoic acid ethyl ester

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:62981-80-0 SDS

62981-80-0Downstream Products

62981-80-0Relevant articles and documents

Tricyclic furo[2, 3-d]pyrimidone compounds and application thereof

-

Paragraph 0096-0097, (2021/07/14)

The invention relates to compounds. Cyanoethyl acetate and chloroacetone with different substituent groups are used as initial raw materials, a cyanoethyl ester compound is generated under the action of sodium ethoxide, then furan compounds are generated

SYNTHESIS OF ESTERS OF 2-SUBSTITUTED 4-KETOPENTANOIC ACIDS BY THE ALKYLATION OF CH-ACIDS USING CHLOROACETONE UNDER PHASE TRANSFER CATALYSIS CONDITIONS

Sizov, A. Yu.,Yanovskaya, L. A.,Dombrovskii, V. A.

, p. 410 - 411 (2007/10/02)

An improved method was developed for the synthesis of ethyl esters of 2-substituted 4-ketopentanoic acids by the alkylation of CH2(X)CO2Et using chloroacetone in the liquid-solid KOH (K2CO3 or Na2CO3)-DMF-PhCH2(Et)3NCl system.

3-Chloro-2-(trimethylsiloxy)-1-propene as an Electrophilic Acetonyl Equivalent. A Novel Regioselective Synthesis of 1,4-Dicarbonyl Compounds

Hosomi, Akira,Shirahata, Akihiko,Araki, Yoshitaka,Sakurai, Hideki

, p. 4631 - 4633 (2007/10/02)

α-Metalated imines, hydrazones, and activated methylene compounds are acetonylated with 3-chloro-2-(trimethylsiloxy)-1-propene in high yield.Highly regioselective acetonylation at either the tertiary or secondary α-carbon of 2-methylcyclohexanone can be carried out by selecting the reaction conditions.

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