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36873-96-8

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36873-96-8 Usage

General Description

2,3,5-triMethoxybenzoic acid is a chemical compound with the molecular formula C10H12O5. It is a white solid that is insoluble in water but soluble in organic solvents. 2,3,5-triMethoxybenzoic acid is a derivative of benzoic acid, with three methoxy groups attached at the 2, 3, and 5 positions of the benzene ring. 2,3,5-triMethoxybenzoic acid has various uses in the pharmaceutical and chemical industries, and it is commonly used as a building block for the synthesis of other organic compounds. It possesses anti-inflammatory and antioxidant properties, making it potentially useful for medical applications. Additionally, it has been found to have potential for use in the formulation of dietary supplements and pharmaceutical formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 36873-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,7 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36873-96:
(7*3)+(6*6)+(5*8)+(4*7)+(3*3)+(2*9)+(1*6)=158
158 % 10 = 8
So 36873-96-8 is a valid CAS Registry Number.

36873-96-8SDS

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 2,3,5-trimethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2,3,5-Trimethoxy-benzoesaeure

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:36873-96-8 SDS

36873-96-8Relevant articles and documents

Synthesis of polyhydroxylated flavonoids bearing a lipophilic decyl tail as potential therapeutic antioxidants

Caldwell, Stuart T.,McPhail, Donald B.,Duthie, Garry G.,Hartley, Richard C.

scheme or table, p. 23 - 33 (2012/03/07)

Antioxidants have potential for the treatment of stroke and neurodegeneration, and chimeric compounds that combine a flavon-3-ol head group related to myricetin and a lipophilic decyl tail are known to protect membranes from oxidative damage at least as well as vitamin E. New flavon-3-ols that are highly hydroxylated in the B ring in ways not found in natural flavon-3-ols and bearing a lipophilic decyl tail have been prepared from trimethoxy-and tetramethoxybenzoic acids accessed by lithiation-carboxylation reactions. Direct enolate acylation was preferred over Baker-Venkataraman rearrangement when there were methoxy groups at both the 2-and the 6-position of the benzoic acid derivatives.

Ga(IIl)-catalyzed cycloisomerization approach to (±)-icetexone and (±)-epi-icetexone

De Jesus Cortez, Felipe,Sarpong, Richmond

supporting information; experimental part, p. 1428 - 1431 (2010/07/03)

"Chemical eqation presented" A Ga(III)-catalyzed cycloisomerization reaction provides expedient access to a benzannulated cycloheptadiene bearing a cyano group, which has been applied to the syntheses of several icetexane diterpenoids including icetexone

A concise and efficient synthesis of protected actinoidic acid, the degradation product of vancomycin

Zhu, Jieping,Beugelmans, Rene,Bigot, Antony,Singh, Girij Pal,Bois-Choussy, Michele

, p. 7401 - 7404 (2007/10/02)

Protected actinoidic acid 2, one of the degradation products of vancomycin, has been efficiently synthesized by a convergent route which is amenable to large scale application as well as to asymmetric synthesis.

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