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Benzoic acid, 2-hydroxy-4-methoxy-3,6-dimethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19104-04-2

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19104-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19104-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,0 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19104-04:
(7*1)+(6*9)+(5*1)+(4*0)+(3*4)+(2*0)+(1*4)=82
82 % 10 = 2
So 19104-04-2 is a valid CAS Registry Number.

19104-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-hydroxy-4-methoxy-3,6-dimethylbenzoate

1.2 Other means of identification

Product number -
Other names 6-Oxy-4-methoxy-2.5-dimethyl-benzoesaeure-methylester

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:19104-04-2 SDS

19104-04-2Relevant academic research and scientific papers

Synthesis of barbacic acid

Long, Yi,Luo, Guo-Yong,Xi, Yin-Kai,Yang, Wu-De,Yu, Xiang

, (2022/01/11)

A new approach for the synthesis of the active barbatic acid has been achieved in eight steps with 22.3% total yield by using commercially available methyl atratate as starting material. This synthesis provides access to multi-gram quantities of barbatic

Isolation, Chemical Modification, and Anticancer Activity of Major Metabolites of the Lichen Parmotrema mesotropum

Mallavadhani, Uppuluri Venkata,Tirupathamma, Reddy Srilakshmi,Sagarika,Ramakrishna, Sistla

, p. 825 - 831 (2019/11/13)

Extensive chromatographic purification of the chloroform–methanol (1:1) extract of the lichen Parmotrema mesotropum led to the isolation of methyl hematommate (1), methyl-2,4-dihydroxy-3,6-dimethylbenzoate (2), orcinol (3), and atranorin (4). The two majo

Preparation of resorcinol derivatives

-

, (2008/06/13)

A process for the preparation of resorcinol derivatives of the general formula I STR1 where R1 is carbalkoxy, nitrile, alkyl or H and R2 to R5 are H or lower alkyl, by reacting the corresponding cyclohexane-1,3-dione (II) with oxygen or an oxygen-containing gas in the presence of a catalytic amount of a copper compound and of from 1 to 10 moles of a hydrogen halide, or from 0.5 to 5 moles of thionyl chloride per mole of II, in an alkanol having from 1 to 6 carbon atoms, tetrahydrofuran or methyl tert.-butyl ether as the solvent, at from 0° to 150 C., without the addition of a significant amount of water to the reaction mixture. Some of the resorcinol derivatives prepared are useful scents with fragrance notes of the character of the odoriferous substance of natural oak moss.

Fulgoicin, A New Depsidone from the Lichen Fulgensia fulgida (Nyl.) Szat.

Mahandru, M. Mohan,Tajbakhsh, Alireza

, p. 2249 - 2252 (2007/10/02)

The synthesis of the depsidone 2,4-dichloro-3-hydroxy-8-methoxy-1,6,9-trimethyl-11H-dibenzodioxepin-11-one (fulgoicin) is described.

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