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735248-42-7

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735248-42-7 Usage

General Description

2H-1-Benzopyran-4-amine, 6-bromo-3,4-dihydro- is a chemical compound with the molecular formula C10H10BrNO. It is a derivative of benzopyran, a heterocyclic compound with a benzene ring fused to a pyran ring. The presence of the bromine atom and the amine group in the molecule imparts specific chemical properties and reactivity. 2H-1-BENZOPYRAN-4-AMINE, 6-BROMO-3,4-DIHYDRO- may be used in organic synthesis, medicinal chemistry, or as a building block for more complex chemical structures. Its specific uses and applications may depend on its chemical and physical properties, which include its solubility, stability, and reactivity in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 735248-42-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,5,2,4 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 735248-42:
(8*7)+(7*3)+(6*5)+(5*2)+(4*4)+(3*8)+(2*4)+(1*2)=167
167 % 10 = 7
So 735248-42-7 is a valid CAS Registry Number.

735248-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-3,4-dihydro-2H-chromen-4-amine

1.2 Other means of identification

Product number -
Other names 2H-1-BENZOPYRAN-4-AMINE,6-BROMO-3,4-DIHYDRO

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:735248-42-7 SDS

735248-42-7Downstream Products

735248-42-7Relevant articles and documents

Microwave-accelerated reductive amination between ketones and ammonium acetate

Dong, Li,Aleem, Saadat,Fink, Cynthia A.

experimental part, p. 5210 - 5212 (2010/11/05)

A new procedure for reductive amination between ketones and ammonium acetate has been developed to access a variety of primary amines. This protocol takes advantage of microwave heating to significantly accelerate the reaction and offers a convenient and effective method to access some interesting amines. This new procedure compares favorably to previously reported approaches in terms of practicality, efficiency, and functional group compatibility.

Cyclic amine derivatives and methods of use

-

Page/Page column 39, (2010/02/14)

Selected compounds are effective for treatment of pain and diseases, such as inflammation mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving pain, inflammation, and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

BICYCLIC COMPOUNDS HAVING BRADYKININ RECEPTORS AFFINITY AND PHARMACEUTICAL COMPOSITIONS THEREOF

-

Page 151, (2008/06/13)

Selected compounds are effective for treatment of pain and diseases, such as inflammation mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and

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