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151583-29-8

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151583-29-8 Usage

General Description

"Methyl 3-(3-bromophenyl)propanoate" is an organic compound that belongs to the ester chemical class. It is also known as methyl (3-bromophenyl)propanoate. This chemical is characterized by a methyl group attached to the carbon of a 3-(3-bromophenyl)propanoate group, which consists of a 3-carbon chain with a bromine-substituted phenyl ring attached. It is commonly used in the pharmaceutical and agrochemical industries as a building block in the synthesis of various compounds. It can also be used in the production of fragrances and as a flavoring agent in the food industry. Overall, "methyl 3-(3-bromophenyl)propanoate" is a versatile compound with a wide range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 151583-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,5,8 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 151583-29:
(8*1)+(7*5)+(6*1)+(5*5)+(4*8)+(3*3)+(2*2)+(1*9)=128
128 % 10 = 8
So 151583-29-8 is a valid CAS Registry Number.

151583-29-8SDS

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-(3-Bromophenyl)Propanoate

1.2 Other means of identification

Product number -
Other names Methyl 3-(3-bromophenyl)propanoate

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:151583-29-8 SDS

151583-29-8Relevant articles and documents

Manganese-catalyzed homogeneous hydrogenation of ketones and conjugate reduction of α,β-unsaturated carboxylic acid derivatives: A chemoselective, robust, and phosphine-free in situ-protocol

Topf, Christoph,Vielhaber, Thomas

, (2021/07/10)

We communicate a user-friendly and glove-box-free catalytic protocol for the manganese-catalyzed hydrogenation of ketones and conjugated C[dbnd]C[sbnd]bonds of esters and nitriles. The respective catalyst is readily assembled in situ from the privileged [Mn(CO)5Br] precursor and cheap 2-picolylamine. The catalytic transformations were performed in the presence of t-BuOK whereby the corresponding hydrogenation products were obtained in good to excellent yields. The described system offers a brisk and atom-efficient access to both secondary alcohols and saturated esters avoiding the use of oxygen-sensitive and expensive phosphine-based ligands.

NEW FYN AND VEGFR2 KINASE INHIBITORS

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Page/Page column 30; 31, (2021/06/22)

The invention relates to a N-phenylcarbamoyl compound of Formula (I) or a pharmaceutically acceptable salt thereof for use in the inhibition of at least one of tyrosine kinase selected from Fyn and VEGFR2 in the treatment of diseases and disorders involved with one or both kinases. (Formula)

Dihydropyridine compound and application thereof to drugs

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Paragraph 0796; 0800-0802, (2019/05/08)

The invention relates to a dihydropyridine compound and application of the dihydropyridine compound serving as a drug, in particular to application of the dihydropyridine compound serving as a drug for treating and preventing hepatitis B. Specifically, the invention relates to the compound shown as the general formula (I) or (Ia) (please see the specifications for the general formula (I) or (Ia))or stereoisomers, tautomer, a nitrogen oxide, solvate, metabolites and medically acceptable salt of the compound or a prodrug of the compound, wherein all variables are defined in the specification. The invention further relates to application of the compound shown as the general formula (I) or (Ia) or enantiomers, non-enantiomers, the tautomer, hydrates, the solvate or the medically acceptable salt of the compound serving as drugs, in particular to application of the compound or the enantiomers, the non-enantiomers, the tautomer, the hydrates, the solvate or the medically acceptable salt of the compound serving as the drugs for treating and preventing hepatitis B.

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