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3-(2-bromo-4-methylphenyl)propanoic acid is an organic compound with the molecular formula C10H11BrO2. It is a derivative of propanoic acid, featuring a 2-bromo-4-methylphenyl group attached to the third carbon of the propanoic acid chain. 3-(2-bromo-4-methylphenyl)propanoic acid is characterized by its bromine atom, which provides it with unique chemical properties, such as increased reactivity and the potential for substitution reactions. The presence of the methyl group on the phenyl ring also influences its chemical behavior and physical properties, such as boiling point and solubility. 3-(2-bromo-4-methylphenyl)propanoic acid may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its versatile structure and reactivity.

829-57-2

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829-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 829-57-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 829-57:
(5*8)+(4*2)+(3*9)+(2*5)+(1*7)=92
92 % 10 = 2
So 829-57-2 is a valid CAS Registry Number.

829-57-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-Brom-4-methyl-phenyl)-propionsaeure

1.2 Other means of identification

Product number -
Other names 3-(2-BROMO-4-METHYLPHENYL)PROPANOIC ACID

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:829-57-2 SDS

829-57-2Relevant academic research and scientific papers

Highly Diastereoselective Synthesis of Medium-Sized Carbocycle-Fused Piperidines via Sequential Hydride Shift Triggered Double C(sp3)-H Bond Functionalization

Kataoka, Miyabi,Otawa, Yuna,Ido, Natsuki,Mori, Keiji

supporting information, p. 9334 - 9338 (2019/11/19)

Herein we report a diastereoselective synthesis of medium-sized carbocycle-fused piperidines via [1,n (n = 6, 7)]-[1,5]-sequential hydride shift triggered double C(sp3)-H bond functionalization. When cinnamylidene malonates having N,N-dibenzyl propylamine moiety were treated with 5 mol % of Yb(OTf)3, a [1,6]-[1,5]-sequential hydride shift/cyclization process proceeded to afford seven-membered carbocycle-fused piperidines with excellent diastereoselectivities. This sequential system was applicable to the synthesis of eight-membered carbocycle-fused piperidines by an unprecedented [1,7]-[1,5]-sequential hydride shift/cyclization process.

Construction of seven-and eight-membered carbocycles by Lewis acid catalyzed C(sp3)-H bond functionalization

Otawa, Yuna,Mori, Keiji

supporting information, p. 13856 - 13859 (2019/11/21)

We achieved a concise construction of seven-and eight-membered carbocycles via Lewis acid catalyzed C(sp3)-H bond functionalization. In these reactions, a quite rare [1,6 (or 7)]-hydride shift/cyclization process proceeded smoothly to afford seven-and eight-membered carbocycles with good chemical yields starting from substrates with high conformational freedom.

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