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α-(Bromomethyl)benzylpropyl ether is an organic compound with the chemical formula C10H13BrO. It is a colorless liquid at room temperature and is soluble in organic solvents. α-(Bromomethyl)benzylpropyl ether is characterized by a benzene ring with a bromine atom attached to the alpha carbon, which is connected to a methyl group and a propyl ether group. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and versatility in organic chemistry. The bromine atom can participate in a range of reactions, such as nucleophilic substitution, making it a valuable building block for the creation of more complex molecules.

52855-10-4

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52855-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52855-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,5 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52855-10:
(7*5)+(6*2)+(5*8)+(4*5)+(3*5)+(2*1)+(1*0)=124
124 % 10 = 4
So 52855-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15BrO/c1-2-8-13-11(9-12)10-6-4-3-5-7-10/h3-7,11H,2,8-9H2,1H3

52855-10-4SDS

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 (2-bromo-1-propoxyethyl)benzene

1.2 Other means of identification

Product number -
Other names 1-Propoxy-2-bromethyl-benzol

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:52855-10-4 SDS

52855-10-4Relevant academic research and scientific papers

Chemoenzymatic intermolecular haloether synthesis

Chen, Shaohang,Dai, Zongjie,Hollmann, Frank,Wang, Qinhong,Wever, Ron,Zeng, Zhigang,Zhang, Jiaan,Zhang, Wuyuan

, (2021/12/21)

A chemoenzymatic method for the synthesis of haloethers is presented. A combination of enzymatic hypohalite synthesis with spontaneous oxidation of alkenes and nucleophilic attack by various alcohols enabled the synthesis of a wide range of haloethers. The reaction system has been characterised and current imitations have been worked out. In the present, aqueous reaction system, hydroxyhalide formation represents the main undesired side reaction. Nevertheless, semi-preparative scale synthesis of a range of haloethers is demonstrated.

Alkoxybromination of olefins using ammonium bromide and oxone

Kumar, Macharla Arun,Naresh, Mameda,Rohitha, Chozhiyath Nappunni,Narender, Nama

supporting information, p. 3121 - 3129 (2014/01/06)

A mild, efficient, and highly regio- and stereoselective method for the methoxy and ethoxy bromination of olefins has been developed using NH 4Br as a bromine source and Oxone as an oxidant. Various kinds of olefins (aromatic, linear, and cyclic olefins) afforded the corresponding alkoxy brominated products in moderate to excellent yields. Taylor & Francis Group, LLC.

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