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1762-63-6

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1762-63-6 Usage

Chemical Family

2-(dimethylamino)-5-phenyl-4(5H)-Thiazolone belongs to the thiazolone family of chemical compounds.

Molecular Weight

The molecular weight of 2-(dimethylamino)-5-phenyl-4(5H)-Thiazolone is 247.32 g/mol.

Fluorescent Properties

2-(dimethylamino)-5-phenyl-4(5H)-Thiazolone is known for its fluorescent properties, which make it useful as a fluorescent probe or tag.

Biological Molecule Detection and Imaging

2-(dimethylamino)-5-phenyl-4(5H)-Thiazolone is used for detecting and imaging biological molecules.

Drug Development

2-(dimethylamino)-5-phenyl-4(5H)-Thiazolone has been studied for its potential use in the development of new drugs for various medical conditions.

Materials Science Applications

2-(dimethylamino)-5-phenyl-4(5H)-Thiazolone has been investigated for its potential applications in materials science, such as in the development of optical brighteners and dyes.

Check Digit Verification of cas no

The CAS Registry Mumber 1762-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1762-63:
(6*1)+(5*7)+(4*6)+(3*2)+(2*6)+(1*3)=86
86 % 10 = 6
So 1762-63-6 is a valid CAS Registry Number.

1762-63-6Downstream Products

1762-63-6Relevant articles and documents

2-Dialkylamino-thiazolin-4-ones from α-Thiocyanato-carboxylic Acid Derivatives

Zimmermann, T.,Fischer, G. W.,Olk, B.

, p. 540 - 546 (2007/10/02)

α-Thiocyanato-acetic acid esters 1 a-c or amide 1 d react with dialkylamine salts of weak acids to give 2-dialkylamino-thiazolin-4-ones 2 a-f.The reaction can be performed using aliphatic alcohols, dipolar aprotic solvents or halogenated hydrocarbons as reaction medium or by heating the educts at 90 deg C without any solvent.According to the latter method, the 5-substituted thiazolinones 2 g, h are obtained from α-thiocyanatopropionic acid ethyl ester (1 d) or α-thiocyanato-phenylacetic acid ethyl ester (1 e) and dimethylamine actetate. - I.r., u.v. and n.m.r. data of the thiazolinones 2 are reported.

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