Welcome to LookChem.com Sign In|Join Free
  • or
Ethanethioic acid, S-[[1-(mercaptomethyl)cyclohexyl]methyl] ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59416-49-8

Post Buying Request

59416-49-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

59416-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59416-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,1 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59416-49:
(7*5)+(6*9)+(5*4)+(4*1)+(3*6)+(2*4)+(1*9)=148
148 % 10 = 8
So 59416-49-8 is a valid CAS Registry Number.

59416-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name S-[[1-(sulfanylmethyl)cyclohexyl]methyl] ethanethioate

1.2 Other means of identification

Product number -
Other names Ethanethioic acid,S-[[1-(mercaptomethyl)cyclohexyl]methyl] 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:59416-49-8 SDS

59416-49-8Downstream Products

59416-49-8Relevant academic research and scientific papers

The Reductive Acylation of Organic Disulfides with Aldehydes under Photochemical and Radical Conditions

Takagi, Makoto,Goto, Setsuo,Tazaki, Masato,Matsuda, Tsutomu

, p. 1982 - 1987 (2007/10/02)

The irradiation of organic disulfides in aldehyde solvents resulted in the reductive fission of the S-S linkage, giving an equimolar mixture of the corresponding thiol and thiol acylate in a good yield.The cyclic disulfides gave mono S-acylated dithiols.The reaction proceeded by means of the photo-initiated radical chain mechanism, and AIBN (azobisisobutyronitrile) effected the same reaction under thermal conditions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 59416-49-8