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2,2'-dichloro-4,4',5,5'-tetrahydroxydiphenylmethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

167634-40-4

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167634-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167634-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,6,3 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 167634-40:
(8*1)+(7*6)+(6*7)+(5*6)+(4*3)+(3*4)+(2*4)+(1*0)=154
154 % 10 = 4
So 167634-40-4 is a valid CAS Registry Number.

167634-40-4Downstream Products

167634-40-4Relevant academic research and scientific papers

Synthesis and antimicrobial activities of halogenated bis(hydroxyphenyl)methanes

Oh, Ki-Bong,Lee, Ji Hye,Lee, Jong Wook,Yoon, Kyung-Mi,Chung, Soon-Chun,Jeon, Heung Bae,Shin, Jongheon,Lee, Hyi-Seung

, p. 945 - 948 (2009)

A series of halophenols was prepared by the reaction of bis(hydroxyphenyl)methanes with effective halogenating agents such as bromine and sulfuryl chloride. One of these compounds, a biologically active halophenol-2,2′,3,3′-tetrabromo-4,4′,5,5′-tetrahydroxydiphenylmethane (1)-frequently isolated from red algae, was synthesized for the first time. Other halophenols included several novel compounds, together with known derivatives that were synthesized from the phenolic intermediates, bis(3,4-dihydroxyphenyl)methane (5) and bis(2-hydroxyphenyl)methane (14). All of the synthesized compounds were tested for antimicrobial activity against Gram-positive, Gram-negative bacteria and fungi. The preliminary structure-activity relationship was investigated in order to determine the essential structural requirements for their antimicrobial activity. Of all these halophenols, 2,2′,3,3′,6-pentabromo-4,4′,5,5′-tetrahydroxydiphenylmethane (8) was found to be the most active against Candida albicans, Aspergillus fumigatus, Trichophyton rubrum, and Trichophyton mentagrophytes while 3,3′,5,5′-tetrachloro-2,2′-dihydroxydiphenylmethane (18) exerted a powerful antibacterial effect against Staphylococcus aureus, Bacillus subtilis, Micrococcus luteus, Proteus vulgaris, and Salmonella typhimurium.

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