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Check Digit Verification of cas no

The CAS Registry Mumber 937-00-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 937-00:
(5*9)+(4*3)+(3*7)+(2*0)+(1*0)=78
78 % 10 = 8
So 937-00-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrClF/c1-4-2-7(10)5(8)3-6(4)9/h2-3H,1H3

937-00-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L07191)  3-(Trifluoromethyl)thiophenol, 97%   

  • 937-00-8

  • 1g

  • 478.0CNY

  • Detail
  • Alfa Aesar

  • (L07191)  3-(Trifluoromethyl)thiophenol, 97%   

  • 937-00-8

  • 5g

  • 1766.0CNY

  • Detail

937-00-8SDS

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 3-(Trifluoromethyl)Thiophenol

1.2 Other means of identification

Product number -
Other names 3-(trifluoromethyl)benzenethiol

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:937-00-8 SDS

937-00-8Relevant articles and documents

Preparation method of 3-trifluoromethyl benzenethiol and 3-methylthio benzotrifluoride

-

Paragraph 0035-0041; 0055-0057, (2019/02/26)

The invention discloses a preparation method of 3-trifluoromethyl benzenethiol and 3-methylthio benzotrifluoride, which belongs to the technical field of chemical synthesis. The invention provides thepreparation method of the 3-trifluoromethyl benzenethio

Solvent-free synthesis of thiophenol using uncatalyzed transfer hydrogenation

Zhou, Shaodong,Qian, Chao,Chen, Xinzhi

experimental part, p. 2432 - 2439 (2012/06/18)

Clean and sustainable transfer hydrogenation for aryl sulfonamides and sulfonyl chlorides is described. The protocol is chemoselective and uses neither catalyst nor solvent.

An efficient synthetic route to aryl thiocyanates from arenesulfinates

Still,Watson

, p. 1355 - 1359 (2007/10/03)

An efficient procedure for the conversion ot the inexpensive and readily available arenesulfinate (sodium) salts in three steps into the corresponding aryl thiocyanates is described. Overall yields are high, and the presence of both electron-with drawing and electron-donating substituents is well tolerated.

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