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7611-60-1

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7611-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7611-60-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,1 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7611-60:
(6*7)+(5*6)+(4*1)+(3*1)+(2*6)+(1*0)=91
91 % 10 = 1
So 7611-60-1 is a valid CAS Registry Number.

7611-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butylsulfanylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-tert-Butylsulfanyl-benzoic acid

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:7611-60-1 SDS

7611-60-1Relevant articles and documents

Steric hindrance effects in tripodal ligands for extraction and back-extraction of Ag+

Hiruta, Yuki,Watanabe, Takafumi,Nakamura, Etsuko,Iwasawa, Naoko,Sato, Hiroyasu,Hamada, Kensaku,Citterio, Daniel,Suzuki, Koji

, p. 9791 - 9798 (2014/03/21)

A novel series of tripodal ligands with thiophenylether arms connected to an anchoring nitrogen has been investigated. Seven tripodal ligands were synthesized by combining methyl, isopropyl, and tert-butyl residue bearing thiophenylether sites as groups w

ORTHO-LITHIATION OF PHENYLTHIOETHERS- AND SOME APPLICATIONS

Horner, L.,Lawson, A. J.,Simons, G.

, p. 353 - 356 (2007/10/02)

A preparative procedure for the ortho-lithiation of phenylthioethers C6H5SR 1 is described.The preparations of 2-alkylthio-substituted benzoic acids 3, benzophenones 5 and phenylphosphines 6 were carried out in isolated yields of 38-73percent, depending on reaction and substituent.The procedure provides a simple route to dithiocatechol and trithiopyrogallol derivatives 7 and 8.The ring-lithiation step gives the best results for R=t-C4H9 (80-90percent) and R=i-C3H7 (70-80percent).R=C2H5 gave lower yields (ca.45percent), while R=CH3 gave principally lithiation at alkyl carbon.

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