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612-76-0

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612-76-0 Usage

General Description

3,3'-Dihydroxybiphenyl, also known as biphenol, is a chemical compound with the molecular formula C12H10O2. It is a colorless solid that is insoluble in water but soluble in organic solvents. It is commonly used as a precursor in the production of various polymers and plastics, and it also has potential applications in the pharmaceutical and agricultural industries. 3,3'-Dihydroxybiphenyl is known to have antioxidant properties and has been studied for its potential health benefits, including its ability to inhibit the growth of certain types of cancer cells. However, it is important to note that 3,3'-Dihydroxybiphenyl can be hazardous if not handled properly, and exposure to high levels of the compound may cause irritation to the skin, eyes, and respiratory system. Therefore, appropriate safety precautions should be taken when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 612-76-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 612-76:
(5*6)+(4*1)+(3*2)+(2*7)+(1*6)=60
60 % 10 = 0
So 612-76-0 is a valid CAS Registry Number.

612-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-hydroxyphenyl)phenol

1.2 Other means of identification

Product number -
Other names [1,1‘-Biphenyl]-3,3‘-diol

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:612-76-0 SDS

612-76-0Relevant articles and documents

Active-alkali metal-promoted reductive cleavage of chlorinated phenols

Azzena, Ugo,Dettori, Giovanna,Pisano, Luisa,Pittalis, Mario,Mangano, Giuseppe,Petretto, Giacomo,Pintore, Giorgio

experimental part, p. 601 - 605 (2012/07/28)

We investigated the degradation of chlorinated phenols under reductive electron transfer reaction conditions. Although Li and Na metal proved useless, activated forms of these metals, either their soluble naphthalene radical anions or 1,2-diarylethane dianions, promoted the degradation of the starting materials to various extents. Additionally, efficient dehalogenation of the sodium salts of several mono-, di-, and tri-chlorophenols was obtained by their reduction with an excess of Na metal and a catalytic amount of naphthalene. Springer-Verlag 2012.

Synthesis of 1-Propyl-3-(3-hydroxyphenyl)piperidine by Regiocontrolled Palladium-Catalyzed Arylation

Nilsson, Kristina,Hallberg, Anders

, p. 4015 - 4017 (2007/10/02)

-

2-amino (or hydroxy) phenethyl-1,2,3,4-tetrahydroisoquinolines as analgesics

-

, (2008/06/13)

Analgesic 1,2,3,4-tetrahydroisoquinolines of the formula (1) STR1 wherein R1 and R2 respectively are hydrogen, hydroxy or alkoxy of 1 to 4 carbon atoms, R3 and R4 respectively are hydrogen or alkyl of 1 to 4 car

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