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1,2-Benzenediol, 4-bromo-5-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18863-72-4

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18863-72-4 Usage

General Description

1,2-Benzenediol, 4-bromo-5-methyl- (9CI) is a chemical compound also known as 4-bromo-5-methylresorcinol. It is a derivative of resorcinol, which is a phenolic compound commonly found in plants. 4-bromo-5-methylresorcinol is used in the production of hair dyes and colorants, as well as in the formulation of pharmaceuticals and cosmetics. It is also used as a reagent in organic synthesis and as an intermediate in the production of other chemicals. 1,2-Benzenediol, 4-bromo-5-methyl- (9CI) has been studied for its potential biological effects and has been found to exhibit antiviral and anticancer properties. However, further research is needed to fully understand its potential applications and risks.

Check Digit Verification of cas no

The CAS Registry Mumber 18863-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,6 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18863-72:
(7*1)+(6*8)+(5*8)+(4*6)+(3*3)+(2*7)+(1*2)=144
144 % 10 = 4
So 18863-72-4 is a valid CAS Registry Number.

18863-72-4SDS

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 4-Bromo-5-methyl-1,2-benzenediol

1.2 Other means of identification

Product number -
Other names 2-Brom-3.5-dihydroxy-toluol

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:18863-72-4 SDS

18863-72-4Relevant articles and documents

A New Secondary Metabolite from Alternaria Alternata: Structure Elucidation and Total Synthesis of Altenuic Acid IV

Kohler, Dominik,Podlech, Joachim

, p. 1748 - 1753 (2019)

A putative intermediate in the biosynthesis of altenuic acids I–III was isolated from Alternaria alternata in the 1950ies and a sample survived over the decades. This resorcylic lactone named altenuic acid IV is a composite of a resorcylic and a muconic a

Total synthesis of decarboxyaltenusin

Warmuth, Lucas,Wei?, Aaron,Reinhardt, Marco,Meschkov, Anna,Schepers, Ute,Podlech, Joachim

supporting information, p. 224 - 228 (2021/02/26)

The total synthesis of decarboxyaltenusin (5'-methoxy-6-methyl-[1,1'-biphenyl]-3,3',4-triol), a toxin produced by various mold fungi, has been achieved in seven steps in a yield of 31% starting from 4-methylcatechol and 1-bromo-3,5-dimethoxybenzene, where

A 4, 5 - dihydroxy -2 - methyl benzoic acid

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Paragraph 0051-0053, (2017/05/03)

The invention discloses a preparation method of 4,5-dihydroxyl-2-methyl benzoic acid and belongs to the fields of fine chemical engineering and medicine intermediates. The preparation method of 4,5-dihydroxyl-2-methyl benzoic acid comprises the following steps: preparing an intermediate III or V by taking 4-methylbenze-1,2-diphenol as a raw material, then preparing an intermediate IV by virtue of the intermediate III or V, then transforming the intermediate IV into an intermediate II, and finally preparing 4,5-dihydroxyl-2-methyl benzoic acid by virtue of the intermediate II. The preparation method of 4,5-dihydroxyl-2-methyl benzoic acid has the advantage that the problems that raw materials are difficult to acquire, byproducts are many, yield is low, cost is high, steps are miscellaneous, safety can not be guaranteed and serious pollution is produced in the prior art are overcome.

Fluorescent probe

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Page/Page column 17-18, (2009/05/29)

A fluorescent probe which is represented by the following formula (I): (wherein, R1 and R2 represent hydrogen atom, or a substituent for trapping proton, a metal ion, or an active oxygen species, or the like; R3 represents

Benzodioxoles: Novel cannabinoid-1 receptor inverse agonists for the treatment of obesity

Alig, Leo,Alsenz, Jochem,Andjelkovic, Mirjana,Bendels, Stefanie,Bénardeau, Agnès,Bleicher, Konrad,Bourson, Anne,David-Pierson, Pascale,Guba, Wolfgang,Hildbrand, Stefan,Kube, Dagmar,Lübbers, Thomas,Mayweg, Alexander V.,Narquizian, Robert,Neidhart, Werner,Nettekoven, Matthias,Plancher, Jean-Marc,Rocha, Cynthia,Rogers-Evans, Mark,R?ver, Stephan,Schneider, Gisbert,Taylor, Sven,Waldmeier, Pius

, p. 2115 - 2127 (2008/12/22)

The application of the evolutionary fragment-based de novo design tool TOPology Assigning System (TOPAS), starting from a known CB1R (CB-1 receptor) ligand, followed by further refinement principles, including pharmacophore compliance, chemical tractabili

NOVEL BENZODIOXOLES

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Page 113-114, (2008/06/13)

The present invention relates to compound of formula (I) Wherein R1, R2, R3, R4, R5, R6, R7, and X are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prophylaxis of diseases, which are associated with the modulation of CB1 receptors.

Rational design of novel photoinduced electron transfer type fluorescent probes for sodium cation

Kenmoku, Suguru,Urano, Yasuteru,Kanda, Koujirou,Kojima, Hirotatsu,Kikuchi, Kazuya,Nagano, Tetuso

, p. 11067 - 11073 (2007/10/03)

We have developed novel fluorescence probes for sodium cation based on photoinduced electron transfer (PeT). In this study, we rationally designed new probes and succeeded in achieving fluorescence enhancement upon sodium ion binding by reducing the HOMO

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