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Methyl 3-(1-Bromomethyl)benzoate, a colorless to light yellow liquid, is a chemical compound belonging to the ester class. It has a molecular formula of C10H11BrO2 and is primarily used as an intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Due to its reactivity, it is also utilized in organic synthesis and as a reagent in chemical reactions. However, it is important to note that Methyl 3-(1-Bromomethyl)benzoate is toxic if swallowed and can cause skin and eye irritation, necessitating proper safety precautions during handling.

50603-99-1

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50603-99-1 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 3-(1-Bromomethyl)benzoate is used as an intermediate in the synthesis of pharmaceuticals for its ability to react with other compounds to form new molecules with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, Methyl 3-(1-Bromomethyl)benzoate serves as an intermediate in the production of various agrochemicals, contributing to the development of new compounds for crop protection and enhancement of agricultural productivity.
Used in Organic Synthesis:
Methyl 3-(1-Bromomethyl)benzoate is utilized in organic synthesis as a versatile reagent, enabling the formation of a wide range of organic compounds through its reactivity with other molecules.
Used as a Reagent in Chemical Reactions:
As a reagent in chemical reactions, Methyl 3-(1-Bromomethyl)benzoate plays a crucial role in facilitating specific transformations and reactions, contributing to the advancement of chemical research and the development of new compounds with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 50603-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,0 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50603-99:
(7*5)+(6*0)+(5*6)+(4*0)+(3*3)+(2*9)+(1*9)=101
101 % 10 = 1
So 50603-99-1 is a valid CAS Registry Number.

50603-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(1-bromoethyl)benzoate

1.2 Other means of identification

Product number -
Other names Methyl-3-(bromaethyl)benzoat

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:50603-99-1 SDS

50603-99-1Relevant academic research and scientific papers

Method for synthesizing alkyne through catalytic asymmetric cross coupling (by machine translation)

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Paragraph 0205-0212; 0270-0272, (2020/01/12)

The invention belongs to the field of, asymmetric synthesis, and discloses a method for catalyzing asymmetric cross- coupling to synthesize: an alkyne, and the L method comprises, the following steps, of A: preparing B a cuprous, salt and C a: ligand; preparing a catalyst; adding a base; reacting the compound with the compound with the compound; and reacting the compound with the compound. Of these, one of them, X is selected from the group consisting of, R halogens. 1 Optionally substituted heteroarylsulfonylcyanamide groups selected from the, group consisting, of optionally substituted, phenyl groups In-flight vehicle, R6 Trialkyl silyl groups or alkyl radicals, R2 Cycloalkyl radicals optionally substituted with an, optionally substituted alkyl, (CH radical2 )n R4 Multi,layer chain, n=0-10,R saw blade4 A group selected, from, the group consisting of phenyl, alkenyl, aralkynyls, noonyloxy,and, noonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylphenyl disiloxy-radicals. R3 A ligand, selected from hydrogen or any of the functional groups, is selected from the group consisting of, hydrogen and any L other functional group. The method, R disclosed by the, A invention has the, advantages of good catalytic, R ’ effect, wide application range. and high catalytic efficiency, and the, method disclosed by the, invention has the. advantages of good catalytic effect, wide application range and high catalytic efficiency. (by machine translation)

SUBSTITUTED DICYANOPYRIDINES AND USE THEREOF

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Paragraph 0518-0522, (2013/08/28)

The present application relates to novel substituted dicyanopyridines, to processes for their preparation, to their use for the treatment and/or prophylaxis of diseases and to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, preferably for the treatment and/or prophylaxis of cardiovascular disorders.

Pharmaceutically active phenylcarboxylic acid derivatives

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, (2008/06/13)

Compounds which antagonize the slow-reacting substance of anaphylaxis or components thereof, e.g., leukotrienes, in warm blooded animals as well as intermediates and methods for their preparation, pharmaceutical compositions and methods for their administration. The compounds are diphenyl carboxylic acids with particular linking groups between the individual phenyl rings and the carboxylic acid moiety. Particular utilities are to relieve asthma and inflammation in man.

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