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693-83-4

693-83-4

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693-83-4 Usage

Chemical Properties

Liquid. Solidifies at 22.2C. Combustible.

Uses

Organic synthesis (formation of sulfonium compounds).

Check Digit Verification of cas no

The CAS Registry Mumber 693-83-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 693-83:
(5*6)+(4*9)+(3*3)+(2*8)+(1*3)=94
94 % 10 = 4
So 693-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H42S/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3

693-83-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Packaging
  • Price
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  • Alfa Aesar

  • (B22560)  Di-n-decyl sulfide, 97%   

  • 693-83-4

  • 10g

  • 629.0CNY

  • Detail

  • Alfa Aesar

  • (B22560)  Di-n-decyl sulfide, 97%   

  • 693-83-4

  • 50g

  • 2500.0CNY

  • Detail

693-83-4SDS

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 1-decylsulfanyldecane

1.2 Other means of identification

Product number -
Other names n-Decyl sulfide

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:693-83-4 SDS

693-83-4Relevant articles and documents

One-pot synthesis of organic disulfides (disulfanes) from alkyl halides using sodium sulfide trihydrate and hexachloroethane or carbon tetrachloride in the poly(ethylene glycol) (PEG-200)

Abbasi, Mohammad,Mohammadizadeh, Mohammad Reza,Moosavi, Hekmat,Saeedi, Narges

, p. 1185 - 1190 (2015/03/31)

Abstract Symmetric disulfides are produced by treating their corresponding organic halides including benzylic, allylic, primary and secondary halides with Na2S·3H2O and C2Cl6 or CCl4 in PEG-200 at room temperature in high yields.

REACTIONS OF ALIPHATIC ALCOHOLS WITH SULFUR AND RED PHOSPHORUS

Mazitova, F. N.,Khairullin, V. K.

, p. 1393 - 1396 (2007/10/02)

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