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5-Bromomethyl-3-(3-nitrophenyl)-isoxazole is a chemical compound with the molecular formula C10H7BrN2O3. It is a derivative of isoxazole that contains a bromomethyl group and a 3-nitrophenyl group. 5-Bromomethyl-3-(3-nitrophenyl)-isoxazole has potential uses in pharmaceutical research and drug development due to its unique structure and potential biological activities.

5301-03-1

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5301-03-1 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
5-Bromomethyl-3-(3-nitrophenyl)-isoxazole is used as a building block for the synthesis of more complex molecules with potential medicinal properties. The presence of the bromomethyl and 3-nitrophenyl groups makes it a valuable component in the development of new drugs.
Used in Medicinal Chemistry:
5-Bromomethyl-3-(3-nitrophenyl)-isoxazole is used as a promising candidate for further exploration in medicinal chemistry. The isoxazole ring structure has been implicated in various biological activities, making 5-Bromomethyl-3-(3-nitrophenyl)-isoxazole a valuable tool for studying and developing new pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 5301-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5301-03:
(6*5)+(5*3)+(4*0)+(3*1)+(2*0)+(1*3)=51
51 % 10 = 1
So 5301-03-1 is a valid CAS Registry Number.

5301-03-1SDS

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 5-(bromomethyl)-3-(3-nitrophenyl)-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 5-bromomethyl-3-(3-nitrophenyl)isoxazole

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:5301-03-1 SDS

5301-03-1Relevant academic research and scientific papers

Synthesis and characterization of 2-Alkyl -5-{4-[(3-nitrophenyl- 5isoxazolyl)methoxy]phenyl}-2H-tetrazoles

Mirzaei,Edjlali

experimental part, p. 685 - 694 (2010/10/20)

Heteroaryl substituted analogs of antirhnoviral (A), was prepared by a convergent approach. 3-Nitrophenyl-5bromooromethylisoxazoles 5a-b were synthesized by [3+2] cycloaddition of 3-(benzoyloxy)-propyne 2 to in situ generated arylnitrile oxides followed by deprotection of cycloadducts 3a-b and bromination of the resulting alcohols 4a-b. Coupling of 3nitrophenyl-5- bromooromethylisoxazoles (5a-b) with 4-[5-(2-alkyl-2H-tetrazolyl)]phenols (6a-d) in N-methylpyrrolidinone under mild conditions afforded a new series of 2-alkyl-5-{4-[1-(3-nitrophenyl-5-isoxazolyl)methyloxy]phenyl}-2H-tetrazoles (7a-h) in high yields. The structures of the synthesized compounds were confirmed by their 1H NMR, Mass spectral, and Elemental Analysis data.

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