Welcome to LookChem.com Sign In|Join Free

CAS

  • or

65398-69-8

Post Buying Request

65398-69-8 Suppliers

Recommended suppliersmore

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

65398-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65398-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,9 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65398-69:
(7*6)+(6*5)+(5*3)+(4*9)+(3*8)+(2*6)+(1*9)=168
168 % 10 = 8
So 65398-69-8 is a valid CAS Registry Number.

65398-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Dimethyl-4-(methylsulfanyl)benzene

1.2 Other means of identification

Product number -
Other names <3,4-Dimethyl-phenyl>-methyl-sulfid

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:65398-69-8 SDS

65398-69-8Relevant articles and documents

Novel dienone-phenol type rearrangement of 4,4-disubstituted cyclohexadienone system using thiosilane

Wada, Yasufumi,Otani, Kouji,Endo, Noriko,Kita, Yasuyuki,Fujioka, Hiromichi

supporting information; experimental part, p. 797 - 799 (2010/06/12)

Thiosilane and a catalytic amount of a Bronsted acid mediate the novel domino-type rearrangement reaction of the 4,4-disubstituted cyclohexadienones to produce the 3,4-disubstituted benzenethioethers; the key step is 1,2-addition of thiosilane to dienone.

The Reaction of Alkyl-substituted Thioanisoles with PCl3 and AlCl3: a Route to Benzothiadiphospholobenzothiadiphosphole Derivatives

Baccolini, Graziano,Mezzina, Elisabetta,Todesko, Paolo Edgardo

, p. 3281 - 3284 (2007/10/02)

The synthesis of benzothiadiphospholobenzothiadiphosphole derivatives starting from alkyl-substituted thioanisoles and PCl3-AlCl3 is reported.The reaction is carried out at reflux in the absence of solvent and the yields are dependent on the starting sulphide.These new heterocycles can be purified by simple filtration on a Florisil column and have been characterized by 1H-, 13C-, (1H)31P-n.m.r. and mass spectroscopy analyses.New unexpected findings are also described.

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

What can I do for you?
Get Best Price

Get Best Price for 65398-69-8