Cas 107401-72-9,[4-AMINO-2-(4-CHLOROANILINO)-1,3-THIAZOL-5-YL](4-CHLOROPHENYL)METHANONE

107401-72-9

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Basic information

Product Name: [4-AMINO-2-(4-CHLOROANILINO)-1,3-THIAZOL-5-YL](4-CHLOROPHENYL)METHANONE
Synonyms: [4-AMINO-2-(4-CHLOROANILINO)-1,3-THIAZOL-5-YL](4-CHLOROPHENYL)METHANONE;5-(4-chlorobenzoyl)-N2-(4-chlorophenyl)-1,3-thiazole-2,4-diamine
CAS NO:107401-72-9
Molecular Formula: C₁₆H₁₁Cl₂N₃OS
Molecular Weight: 364.25
EINECS: N/A
Product Categories: N/A
Mol File: 107401-72-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [4-AMINO-2-(4-CHLOROANILINO)-1,3-THIAZOL-5-YL](4-CHLOROPHENYL)METHANONE(CAS DataBase Reference)
NIST Chemistry Reference: [4-AMINO-2-(4-CHLOROANILINO)-1,3-THIAZOL-5-YL](4-CHLOROPHENYL)METHANONE(107401-72-9)
EPA Substance Registry System: [4-AMINO-2-(4-CHLOROANILINO)-1,3-THIAZOL-5-YL](4-CHLOROPHENYL)METHANONE(107401-72-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
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HazardClass: N/A
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Hazardous Substances Data: 107401-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107401-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,0 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 107401-72:
(8*1)+(7*0)+(6*7)+(5*4)+(4*0)+(3*1)+(2*7)+(1*2)=89
89 % 10 = 9
So 107401-72-9 is a valid CAS Registry Number.

107401-72-9Upstream product

107401-72-9Downstream Products

107401-72-9Relevant academic research and scientific papers

DIAMINOTHIAZOLE COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Paragraph 00163; 00164; 00165; 00173, (2018/05/27)

The disclosure relates to diaminothiazole derivatives of formula (I) where the variables are as defined herein, pharmaceutical compositions containing such compounds, and methods for the use of such compounds and compositions for the treatment of hyperpro

One-pot sequential multicomponent route to 2,4-diaminothiazoles - A facile approach to bioactive agents for cancer therapeutics

Sreejalekshmi, Kumaran G.,Rajasekharan, Kallikat N.

supporting information; experimental part, p. 3627 - 3629 (2012/09/22)

A facile one-pot sequential three-component route to 2,4-diaminothiazoles is reported. The new approach employs the mildest reaction conditions and commercially available reagents to generate diverse 2-alkyl/arylamino-4-amino-5- aroyl/heteroylthiazoles in short reaction times, good yield, and purity.

THIAZOLE AND THIOPHENE ANALOGUES, AND THEIR USE IN TREATING AUTOIMMUNE DISEASES AND CANCERS

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Page/Page column 89, (2008/06/13)

Thiazole and thiophene compounds are disclosed having utility in treating inflammatory conditions, immunoinflammatory conditions, autoimmune diseases, and cancers. Methods for the synthesis of these compounds are also disclosed.

Studies on the Synthesis of 5-Acyl-2,4-diaminothiazoles from Amidinothioureas

Rajasekharan, K. N.,Nair, K. P.,Jenardanan, G. C.

, p. 353 - 355 (2007/10/02)

1-Alkyl or aryl-3-amidinothioureas with or without substituents on the amidino moiety react with α-haloketones to yield 5-acyl-2,4-diaminothiazoles.

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