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2150-42-7

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2150-42-7 Usage

General Description

Methyl 2,3-dimethoxy benzoate, also known as veratraldehyde methyl ether, is an organic compound with the chemical formula C10H12O4. It is a colorless to slightly yellow liquid with a sweet, floral odor. This chemical is commonly used in the fragrance and flavor industries, as well as in the production of pharmaceuticals and agrochemicals. It is often employed as a flavoring agent in food and beverages, and as a fragrance ingredient in perfumes and personal care products. Methyl 2,3-dimethoxy benzoate is also utilized in the synthesis of various pharmaceutical intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 2150-42-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2150-42:
(6*2)+(5*1)+(4*5)+(3*0)+(2*4)+(1*2)=47
47 % 10 = 7
So 2150-42-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O4/c1-12-8-6-4-5-7(9(8)13-2)10(11)14-3/h4-6H,1-3H3

2150-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2,3-dimethoxybenzoate

1.2 Other means of identification

Product number -
Other names 2,3-dimethoxy-benzoic acid methyl ester

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:2150-42-7 SDS

2150-42-7Relevant articles and documents

Dihydroxylation Studies of Isoquinolinones: Synthesis of the EF-Ring of Lysolipin i

Heinemann, Maximilian J. B.,Voigt, Thomas,Menche, Dirk

, p. 465 - 474 (2021/10/25)

Inspired by the potent polycyclic xanthone antibiotic lysolipin I, a general study on asymmetric dihydroxylation reactions of variously substituted isoquinolinones was performed. Different isoquinolinones were efficiently prepared, either by a Pomeranz-Fritsch type condensation or a Curtius rearrangement. Under a broad variety of conventional oxygenation procedures, they proved very unreactive. However, either by suitable substitution of the appending aromatic ring or more forcing conditions a dihydroxylation could finally be performed, which allowed the synthesis of the EF-ring of lysolipin I.

Facile preparation of aromatic esters from aromatic bromides with ethyl formate or DMF and molecular iodine via aryllithium

Ushijima, Sousuke,Moriyama, Katsuhiko,Togo, Hideo

experimental part, p. 4701 - 4709 (2012/07/28)

Various aromatic bromides were treated with n-BuLi and subsequently with ethyl formate, followed by the reaction with ethanol and molecular iodine in the presence of K2CO3 to provide the corresponding aromatic ethyl esters in good yields. Moreover, aromatic bromides could be transformed into the corresponding aromatic methyl esters in good yields by the treatment with n-BuLi and subsequently with DMF, followed by the reaction with methanol, molecular iodine, and K2CO3. Some aromatics could be also converted into the corresponding aromatic esters in good yields by the treatment with n-BuLi, and subsequently with ethyl formate or DMF, followed by the reaction with molecular iodine and K2CO3. The present reactions offer a novel route for the transition-metal-free, carbon-monoxide-free, and therefore environmentally benign one-pot conversion of aromatic bromides and aromatics into aromatic esters.

COMPOUNDS WITH 7-MEMBER CYCLE AND THE PHARMACEUTICAL USE THEREOF FOR PREVENTING AND TREATING DIABETES AND METABOLISM SYNDROME

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Page/Page column 33, (2010/07/06)

The invention discloses a new use of a class of heptacyclic compounds in the preparation of formulations for the prevention and treatment of diabetes and metabolic syndromes; the present invention also discloses a new class of heptacyclic compounds; the present invention also discloses a process for preparing the heptacyclic compounds and a composition containing the same. The heptacyclic compounds of the present invention can be used to effectively preventing or treating diseases such as diabetes and metabolic syndromes.

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