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135525-78-9

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  • 3-[(4,7-dichloro-1,3-benzoxazol-2-yl)methylamino]-5-ethyl-6-methyl-1H-pyridin-2-one

    Cas No: 135525-78-9

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135525-78-9 Usage

Molecular Structure

Includes a benzoxazolylmethylamino group and a pyridinone group

Synthesis

Achieved through multiple chemical reactions

Usage

Employed in research and pharmaceutical applications

Potential Medicinal Properties

May exhibit antimicrobial, antioxidant, or anti-inflammatory effects

Biological Activities

Under study for various therapeutic uses

Complex Structure Advantage

Potential for binding to specific biological targets

Drug Development

Promising candidate for pharmaceutical development

Applications in Research

Potential uses in chemical research and development of new materials

Check Digit Verification of cas no

The CAS Registry Mumber 135525-78-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,2 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135525-78:
(8*1)+(7*3)+(6*5)+(5*5)+(4*2)+(3*5)+(2*7)+(1*8)=129
129 % 10 = 9
So 135525-78-9 is a valid CAS Registry Number.

135525-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4,7-dichloro-1,3-benzoxazol-2-yl)methylamino]-5-ethyl-6-methyl-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 3-{[(4,7-dichlorobenzoxazol-2-yl)methyl]amino}-5-ethyl-6-methyl-2-(1H)-pyridinone

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:135525-78-9 SDS

135525-78-9Downstream Products

135525-78-9Relevant articles and documents

The synthesis of several tritiated non-nucleoside, HIV-1 reverse transcriptase inhibitors

Hamill, Terence G.,Brenner, Nancy J.,Eng, Wai-Si,Burns, H. Donald

, p. 319 - 327 (2007/10/03)

The synthesis of three tritiated reverse transcriptase inhibitors is described herein. These compounds contained the benzoxazole ring linked to a 2-pyridinone ring by an aminomethylene group. The tritiated compounds were synthesized by hydrogenolysis of bromobenzoxazole precursors. The final tritiated compounds had specific activities ranging from 3-10 Cl/mmol.

2-pyridinone derivatives: A new class of nonucleoside, HIV-1-specific reverse transcriptase inhibitors [3]

Saari,Hoffman,Wai,Fisher,Rooney,Smith,Thomas,Goldman,O'Brien,Nunberg,Quintero,Schleif,Emini,Stern,Anderson

, p. 2922 - 2925 (2007/10/02)

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