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30493-40-4

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30493-40-4 Usage

Type of compound

Heterocyclic compound

Structure

Contains a pyridine ring fused to an imidazole ring

Additional functional group

Ketone group attached to the pyridine ring

Presence of a substituent

Chloro substituent on the pyridine ring

Relevance in the field

Medicinal chemistry and pharmaceutical research

Potential

Possesses potential biological activity

Application

Utilized in the development of new drugs

Influence of chloro substituent

Adds to its reactivity and can influence its pharmacological properties

Versatility

Ketone functional group allows for further chemical modifications

Purpose of modifications

To enhance biological activity and selectivity

Check Digit Verification of cas no

The CAS Registry Mumber 30493-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,9 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30493-40:
(7*3)+(6*0)+(5*4)+(4*9)+(3*3)+(2*4)+(1*0)=94
94 % 10 = 4
So 30493-40-4 is a valid CAS Registry Number.

30493-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-chloro-5H-imidazo[2,1-b][1,3]oxazin-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names -

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:30493-40-4 SDS

30493-40-4Relevant articles and documents

DERIVATIVES OF 4-(IMIDAZO[L,2-A]PYRIDIN-3-YL)-N-(PYRIDINYL)PYRIMIDIN- 2-AMINE AS THERAPEUTIC AGENTS

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Paragraph 0083-0084; 0096; 00101, (2021/01/29)

A novel class of heteroaryl compounds for use in the prevention and/or treatment of proliferative diseases and conditions including cancers. The compounds are considered to be capable of inhibiting cell proliferation by inhibiting the activity of FLT3 and its mutant forms and/or other protein kinases such as CDKs. The compounds have the general structure I:

A 2-amino-thiazole compounds (by machine translation)

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Paragraph 0163, (2016/10/08)

The present invention relates to the technical field of pharmaceutical chemistry, particularly relates to a 2-amino thiazole compound or its pharmaceutically acceptable salts, its preparation method, and pharmaceutical compositions containing such compounds and its application in the preparation of antineoplastic. (by machine translation)

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