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Benzoic acid, 3-(methoxymethyl)-, methyl ester, also known as methyl 3-(methoxymethyl)benzoate, is an organic compound with the chemical formula C10H12O3. It is a colorless liquid with a molecular weight of 180.20 g/mol. This ester derivative of benzoic acid features a methoxymethyl group at the 3-position and a methyl ester group at the carboxylic acid end. It is synthesized by reacting 3-hydroxybenzyl alcohol with methyl iodide and sodium hydride, followed by esterification with methanol. Benzoic acid, 3-(methoxymethyl)-, methyl ester is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the synthesis of fragrances and flavorings. Due to its reactivity and functional groups, it is an important building block in organic synthesis, particularly in the preparation of complex molecules with potential biological activity.

1515-87-3

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1515-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1515-87-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1515-87:
(6*1)+(5*5)+(4*1)+(3*5)+(2*8)+(1*7)=73
73 % 10 = 3
So 1515-87-3 is a valid CAS Registry Number.

1515-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(methoxymethyl)benzoate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1515-87-3 SDS

1515-87-3Relevant academic research and scientific papers

ALK5 INHIBITORS

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, (2020/07/07)

The present disclosure provides inhibitors of activin receptor-like kinase 5 (ALK5). Also disclosed are methods to modulate the activity of ALK5 and methods of treatment of disorders mediated by ALK5.

Birch Reductive Alkylation of Methyl m-(Hydroxymethyl)benzoate Derivatives and the Behavior of o- and p-(Hydroxymethyl)benzoates under Reductive Alkylation Conditions

Fretz, Samuel J.,Hadad, Christopher M.,Hart, David J.,Vyas, Shubham,Yang, Dexi

, p. 83 - 92 (2013/03/29)

Birch reductive alkylation of methyl m-(hydroxymethyl)benzoate derivatives, using lithium in ammonia-tetrahydrofuran in the presence of tertbutyl alcohol, can be achieved without significant loss of benzylic oxygen substituents. Similar treatment of o- and p-(hydroxymethyl)benzoate derivatives results largely in loss of benzylic oxygen substituents. The results are rationalized by computations describing electron density patterns in the putative radical anion intermediate involved in these reactions.

DERIVATIVES OF 2-PYRIDIN-2-YL-PYRAZOL-3(2H)-ONE, PREPARATION AND THERAPEUTIC USE THEREOF AS HIF ACTIVATORS

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Page/Page column 17, (2011/12/13)

The present invention relates to novel substituted dihydropyrazolone derivatives, to their preparation and to their therapeutic use as activators of the transcription factor HIF.

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