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26507-91-5

26507-91-5

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26507-91-5 Usage

General Description

2-Methoxy-3-methylbenzoic acid, also known as guaiacol-3-carboxylic acid, is a chemical compound with the molecular formula C9H10O3. It is a derivative of benzoic acid, with a methoxy group and a methyl group attached to the benzene ring. 2-Methoxy-3-methylbenzoic acid is commonly used as a flavoring agent in the food industry and as a fragrance ingredient in the cosmetics and personal care products industry. It is also used in organic synthesis and as a starting material for the production of pharmaceuticals and other fine chemicals. 2-Methoxy-3-methylbenzoic acid is a white to off-white crystalline solid with a slightly sweet, phenolic odor. It is considered to be relatively stable under normal conditions and is not known to pose significant health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 26507-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,0 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26507-91:
(7*2)+(6*6)+(5*5)+(4*0)+(3*7)+(2*9)+(1*1)=115
115 % 10 = 5
So 26507-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c1-6-4-3-5-7(9(10)11)8(6)12-2/h3-5H,1-2H3,(H,10,11)

26507-91-5SDS

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-METHOXY-3-METHYLBENZOIC ACID

1.2 Other means of identification

Product number -
Other names Methylaether-o-kresotinsaeure

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:26507-91-5 SDS

26507-91-5Relevant articles and documents

Fluorescent macrocyclic chemosensor for Zn(II) detection at alkaline pH values

Ambrosi, Gianluca,Formica, Mauro,Fusi, Vieri,Giorgi, Luca,Micheloni, Mauro,Paderni, Daniele

, (2020/01/25)

The new macrocyclic ligand L (28,29-dimethoxy-27-oxa-8,11,14,17,25,26-hexaazatetracyclo[22.2.1.1(2,6).1(19,23)]nonacosa-2,4,6(28),19,21,23(29),24,26(1)-octaene) has been synthesised. It contains a tetramine chain and the 2,5-bis(2-methoxy-3-metyl-phenyl)-

Stereoselective Synthesis of Isochromanones by an Asymmetric Ortho-Lithiation Strategy: Synthetic Access to the Isochromanone Core of the Ajudazols

Essig, Sebastian,Menche, Dirk

, p. 1943 - 1966 (2016/03/15)

Full details on the design, development, and application of a highly stereoselective strategy for the synthesis of isochromanones are reported. The method is based on an asymmetric ortho lithiation with aldehyde electrophiles and utilizes the chiral memor

Metal triflate-catalyzed cyclization of arylvinylcarbinols: Formal synthesis of (±)-dichroanone and (±)-taiwaniaquinone H

Kakde, Badrinath N.,De, Subhadip,Dey, Dhananjay,Bisai, Alakesh

, p. 8176 - 8179 (2013/09/02)

A formal synthesis of diterpenoids viz. the taiwaniaquinoids (±)-dichroanone (1a) and (±)-taiwaniaquinone H (1b) possessing an all carbon quaternary stereocenter has been reported. The key step involves a metal triflate-catalyzed cyclization of arylvinylc

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