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2-(Benzyloxy)-4-bromo-1-chlorobenzene is a benzene derivative featuring a benzene ring with a benzyloxy group and a bromine atom at the 2 and 4 positions, respectively, and a chlorine atom at the 1 position. This chemical compound is known for its reactivity and potential biological activity, making it a valuable component in organic synthesis and pharmaceutical research.

903579-12-4

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903579-12-4 Usage

Uses

Used in Organic Synthesis:
2-(Benzyloxy)-4-bromo-1-chlorobenzene is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure and reactivity allow for the development of a wide range of chemical compounds with various applications.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-(Benzyloxy)-4-bromo-1-chlorobenzene is utilized as a precursor in the production of various pharmaceuticals. Its potential biological activity and ability to be modified into different molecular structures make it a promising candidate for the development of new drugs.
Used in Agrochemical Production:
2-(Benzyloxy)-4-bromo-1-chlorobenzene is also used as a precursor in the production of agrochemicals. Its chemical properties and reactivity contribute to the synthesis of compounds that can be used in agriculture for pest control and crop protection.
Safety Precautions:
It is important to handle 2-(Benzyloxy)-4-bromo-1-chlorobenzene with caution due to its potential hazardous properties. It should be used in a controlled environment by trained professionals to ensure safety and minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 903579-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,3,5,7 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 903579-12:
(8*9)+(7*0)+(6*3)+(5*5)+(4*7)+(3*9)+(2*1)+(1*2)=174
174 % 10 = 4
So 903579-12-4 is a valid CAS Registry Number.

903579-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Benzyloxy)-4-bromo-1-chlorobenzene

1.2 Other means of identification

Product number -
Other names 4-bromo-1-chloro-2-phenylmethoxybenzene

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:903579-12-4 SDS

903579-12-4Relevant academic research and scientific papers

Compounds and methods of use

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Page/Page column 610-611, (2021/08/04)

Compounds are provided according to Formula (I): and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof; wherein X1, X2, X3, X4, Y, A, L1, L2, R1, R2, R5, m and n are as defined herein. Compounds of the present invention are contemplated useful for the prevention and treatment of a variety of conditions.

ISOQUINOLINONE COMPOUND AND USE THEREOF IN PREPARATION OF ANTIVIRAL DRUGS

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Paragraph 0142; 0143; 0187, (2019/06/12)

Disclosed is an isoquinolinone compound as shown in Formula (I) or a stereoisomer, pharmaceutically acceptable salt, solvate or crystal thereof, and a preparation method thereof, and use thereof in the preparation of drugs for treating or preventing viral infectious diseases caused by the hepatitis B virus (HBV) and other viruses, in particular, use thereof in drugs as HBV surface antigen inhibitors and HBV DNA production inhibitors. The compound has a significant activity in inhibiting hepatitis B surface antigen and hepatitis B DNA, and is possible to significantly improve the probability of curing hepatitis B by administration in combination with nucleoside drugs or other drugs in the future, and has good clinical application prospects.

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