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52458-11-4

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52458-11-4 Usage

Derivative of

Bromobenzene

Functional groups

Benzyl ether group, t-butyl group

Attached to

1-position (benzyl ether), 4-position (t-butyl)

Common use

Organic synthesis reagent

Specific reactions

Suzuki coupling, Heck reaction

Building block for

Pharmaceuticals, agrochemicals, fine chemicals

Physical state

Colorless to pale yellow liquid

Solubility

Insoluble in water, soluble in organic solvents (ethanol, ether)

Hazardous nature

Potential for skin, eye, and respiratory tract irritation

Check Digit Verification of cas no

The CAS Registry Mumber 52458-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,5 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52458-11:
(7*5)+(6*2)+(5*4)+(4*5)+(3*8)+(2*1)+(1*1)=114
114 % 10 = 4
So 52458-11-4 is a valid CAS Registry Number.

52458-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-4-tert-butyl-1-phenylmethoxybenzene

1.2 Other means of identification

Product number -
Other names 1-Benzyloxy-2-bromo-4-t-butylbenzene

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:52458-11-4 SDS

52458-11-4Relevant articles and documents

Research on unique masked ortho-benzoquinone, monohemiaminal: Synthesis and reactions

Matsumoto, Yuri,Nakamura, Akihiko,Saito, Emi,Nakada, Masahisa

, p. 232 - 252 (2019/04/27)

Synthesis of ortho-benzoquinone monohemiaminals via the oxidative dearomatization/O-cyclization cascades of phenols bearing an ortho substituent derived from an amino alcohol with PIDA is described. The cascade reactions of substrates bearing a chiral substituent were found to proceed in a stereoselective manner. The Diels-Alder reactions of the ortho-benzoquinone monohemiaminals proceed in a highly stereoselective manner. The oxidative dearomatization/O-cyclization cascade affording the ortho-benzoquinone monohemiaminal had never been reported; hence, there is still ample scope for further investigation.

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