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6284-54-4

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6284-54-4 Usage

Synonyms

SU4312

Chemical Class

Synthetic indolinone derivative

+ Anti-angiogenic

SU4312 has been studied for its ability to inhibit the formation of new blood vessels, which is crucial for cancer progression.

+ Anti-tumor

The compound has been investigated for its potential anti-tumor properties.

+ Inhibits VEGF receptor tyrosine kinases

SU4312 has been found to inhibit the activity of vascular endothelial growth factor (VEGF) receptor tyrosine kinases, which are involved in the growth and spread of cancer.

Therapeutic Potential

SU4312 has been studied for its potential therapeutic effects in the development of new anti-cancer drugs and has shown promise in preclinical studies.

Check Digit Verification of cas no

The CAS Registry Mumber 6284-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6284-54:
(6*6)+(5*2)+(4*8)+(3*4)+(2*5)+(1*4)=104
104 % 10 = 4
So 6284-54-4 is a valid CAS Registry Number.

6284-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(5-amino-2-methylphenyl)methyl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-(5-amino-2-methylbenzyl)-1h-isoindole-1,3(2h)-dione

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:6284-54-4 SDS

6284-54-4Relevant articles and documents

A Comparison of the Reactions of Some Ethyl N-Arylcarbamates with Those of the Corresponding Acetanilides. II Amidomethylation with N-Hydroxymethylphthalimide

Rosevear, Judi,Wilshire, John F. K.

, p. 339 - 353 (2007/10/02)

The reactions of some ethyl N-arylcarbamates and of the corresponding acetanilides towards 1 equiv. of N-hydroxymethylphthalimide in concentrated sulfuric acid at 50 deg C have been compared with one another.In the case of certain para-substituted compoun

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