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1191-67-9

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1191-67-9 Usage

Uses

1,10-Decanedithiol is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1191-67-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1191-67:
(6*1)+(5*1)+(4*9)+(3*1)+(2*6)+(1*7)=69
69 % 10 = 9
So 1191-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H22S2/c11-9-7-5-3-1-2-4-6-8-10-12/h11-12H,1-10H2

1191-67-9 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L11064)  1,10-Decanedithiol, 95%   

  • 1191-67-9

  • 5g

  • 418.0CNY

  • Detail
  • Alfa Aesar

  • (L11064)  1,10-Decanedithiol, 95%   

  • 1191-67-9

  • 25g

  • 1546.0CNY

  • Detail

1191-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,10-Decanedithiol

1.2 Other means of identification

Product number -
Other names 1,10-Decanedithiol

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:1191-67-9 SDS

1191-67-9Relevant articles and documents

-

Hull et al.

, p. 513 (1948)

-

Process for preparation of dithiols

-

, (2008/06/13)

The invention relates to the synthesis of dithiols and more particularly that of α,ω-dithiols having 5 to 20 carbon atoms. The process according to the invention comprises reacting a di-(tertiary-alkylthio)alkane with hydrogen sulphide in the presence of a solid acid catalyst. The alkane dithiol is obtained selectively and a tertiary-alkyl mercaptan is obtained as by-product. It is possible to reuse the latter in a cyclical process to produce the original di-(tertiary-alkylthio)alkane.

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