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Pentanal, 3-mercapto-4-oxo- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62118-10-9

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62118-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62118-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,1 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62118-10:
(7*6)+(6*2)+(5*1)+(4*1)+(3*8)+(2*1)+(1*0)=89
89 % 10 = 9
So 62118-10-9 is a valid CAS Registry Number.

62118-10-9SDS

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 4-oxo-3-sulfanylpentanal

1.2 Other means of identification

Product number -
Other names Pentanal,3-mercapto-4-oxo

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:62118-10-9 SDS

62118-10-9Upstream product

62118-10-9Downstream Products

62118-10-9Relevant academic research and scientific papers

Process for producing 2-mercapto-1,4-diones

-

, (2008/06/13)

Process for producing 2-mercapto alkane-1,4-diones comprising the steps of: I. Providing a 2-ene-1,4-dione having the structure: STR1 ii. Intimately admixing said 2-ene-1,4-dione with a sulfur compound having the formula: thereby providing a substituted or unsubstituted 2-thia substituted alkane 1,4 dione having the structure: STR2 iii. Hydrolyzing said 2-thia substituted 1,4 dione thereby forming a 2-mercapto alkane-1,4-dione having the structure: STR3 wherein R3 is selected from the group consisting of acyl and aroyl, wherein R2 is lower alkyl; and wherein R4 and R6 are the same or different and are selected from the group consisting of hydrogen and lower alkyl; wherein when R1 is hydrogen, the reaction (ii) is carried out in the presence of an organic base; and wherein when R1 is lower alkyl, the reaction (ii) is carried out in the absence of catalyst or in the presence of catalyst. Examples of such organic bases are piperidine, pyridine, triethyl amine, quinoline or alpha-picoline.

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