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N-(4-biphenyl-4-yl-1,3-thiazol-2-yl)-4-oxo-4H-chromene-3-carboxamide is a complex organic compound with a molecular formula of C24H15N3O3S. It is characterized by a biphenyl group attached to a 1,3-thiazole ring, which in turn is connected to a chromene-3-carboxamide moiety. N-(4-biphenyl-4-yl-1,3-thiazol-2-yl)-4-oxo-4H-chromene-3-carboxamide is known for its potential applications in medicinal chemistry, particularly as a scaffold for the development of new drugs. Its structure allows for a range of chemical modifications, making it a versatile starting point for the synthesis of various bioactive molecules. The compound's specific properties and potential uses are under investigation, with a focus on its interactions with biological targets and its pharmacological effects.

6263-82-7

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6263-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6263-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6263-82:
(6*6)+(5*2)+(4*6)+(3*3)+(2*8)+(1*2)=97
97 % 10 = 7
So 6263-82-7 is a valid CAS Registry Number.

6263-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-oxo-N-[4-(4-phenylphenyl)-1,3-thiazol-2-yl]chromene-3-carboxamide

1.2 Other means of identification

Product number -
Other names 2,2',4,4',6,6'-Hexamethyl-4,4'-bi-4H-pyran

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:6263-82-7 SDS

6263-82-7Upstream product

6263-82-7Downstream Products

6263-82-7Relevant academic research and scientific papers

On the Electrochemistry of Pyrylium Ions at the Mercury Electrode. I. Aliphatically Substituted Ions in Acetonitrile

Garrard, W. Neil,Thomas, Francis G.

, p. 1983 - 1989 (2007/10/02)

The electrochemical behaviour of 2,4,6-trimethyl- and 2,4,6-tri-t-butyl-pyrydium tetrafluoroborates in acetonitrile is reported.Both compounds undergo a reversible, one-electron reduction followed by dimerization of the pyranyl radical.In the case of the trimethyl radical the dimerization is irreversible whereas the tri-t-butyl radical is in equilibrium with its dimer.Rate constants for the chemical reactions have been determined.

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