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3,5-bis(benzylthio)pentanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102162-40-3

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102162-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102162-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,6 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102162-40:
(8*1)+(7*0)+(6*2)+(5*1)+(4*6)+(3*2)+(2*4)+(1*0)=63
63 % 10 = 3
So 102162-40-3 is a valid CAS Registry Number.

102162-40-3Relevant academic research and scientific papers

DEUTERATED DERIVATIVES OF 6,8-BIS(BENZYLSULFANYL)OCTANOIC ACID

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, (2021/02/12)

The invention provides new deuterated derivatives of 6,8-bis(benzylsulfanyl)octanoic acid, pharmaceutical compositions thereof, and methods for treating cancer with the new compositions.

1,2-DITHIOLANE AND DITHIOL COMPOUNDS USEFUL IN TREATING MUTANT EGFR-MEDIATED DISEASES AND CONDITIONS

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, (2018/08/12)

Compositions of the invention comprise 1,2-dithiolane, dithiol and related compounds useful as therapeutic agents for the treatment and prevention of diseases and conditions associated with aberrant EGFR activity.

1,2-DITHIOLANE AND DITHIOL COMPOUNDS USEFUL IN TREATING MUTANT EGFR-MEDIATED DISEASES AND CONDITIONS

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, (2018/08/09)

Compositions of the invention comprise 1,2-dithiolane, dithiol and related compounds useful as therapeutic agents for the treatment and prevention of diseases and conditions associated with aberrant EGFR activity.

Synthesis and Biological Activity of 1,2-Dithiolanes and 1,2-Dithianes Bearing a Nitrogen-containing Substituent

Uneme, Hideki,Mitsudera, Hiroyuki,Kamikado, Toshiya,Kono, Yoshiaki,Manabe, Yukiaki,Numata, Mitsuo

, p. 2023 - 2033 (2007/10/02)

A series of 1,2-dithiolanes, 1,2-dithianes and related compounds bearing a nitrogen-containing substituent were synthesized and their pesticidal activity was tested.A new general synthetic route to 1,2-dithiolanes was established from 1,3-diols.A variation in the position and character of the nitrogen atom is shown to be allowable to some extent for promoting insecticidal activity, unlike the case of sulfur atoms.Most compounds showed acaricidal activity, the strongest being displayed by cis-3,5-bis(dimethylaminomethyl)-1,2-dithiolane.

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