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Phenol, 2,2'-[1,2-ethanediylbis(thio)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107777-29-7

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107777-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107777-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,7 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107777-29:
(8*1)+(7*0)+(6*7)+(5*7)+(4*7)+(3*7)+(2*2)+(1*9)=147
147 % 10 = 7
So 107777-29-7 is a valid CAS Registry Number.

107777-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(2-hydroxyphenyl)sulfanylethylsulfanyl]phenol

1.2 Other means of identification

Product number -
Other names 2,2'-Aethandiyldimercapto-di-phenol

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:107777-29-7 SDS

107777-29-7Downstream Products

107777-29-7Relevant academic research and scientific papers

Structural features of a sulfur-containing group 4 metalla[11]-crown-4 derivative

Snell, Alexander,Kehr, Gerald,Wibbeling, Birgit,Fr?hlich, Roland,Erker, Gerhard

, p. 838 - 842 (2007/10/03)

Treatment of the ligand system (o-C6H4OH)-S-CH 2-CH2-S-(o-C6H4-OH) (2a) with TiCl4 gave the metalla-crown ether derivative [(-S-CH 2-CH2-S-)(o-C6

AROMATIZATION OF 2-ALKYLTHIO(ARYLTHIO)-CYCLOHEXANONES DURING BROMINATION

Kudryavtsev, K. V.,Lonina, N. N.,Samoshin, V. A.

, p. 1425 - 1431 (2007/10/03)

When treated with bromine or N-bromosuccinimide under mild conditions, 2-alkylthio- and 2-arylthiocyclohexanones are converted into the corresponding o-alkylthio- and o-arylthiophenols.

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