Cas 85545-47-7,(4-Chloro-phenyl)-[4-methyl-5-(2-phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-thiazol-2-yl]-amine

85545-47-7

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Basic information

Product Name: (4-Chloro-phenyl)-[4-methyl-5-(2-phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-thiazol-2-yl]-amine
Synonyms:
CAS NO:85545-47-7
Molecular Formula:
Molecular Weight: 462.039
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (4-Chloro-phenyl)-[4-methyl-5-(2-phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-thiazol-2-yl]-amine(CAS DataBase Reference)
NIST Chemistry Reference: (4-Chloro-phenyl)-[4-methyl-5-(2-phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-thiazol-2-yl]-amine(85545-47-7)
EPA Substance Registry System: (4-Chloro-phenyl)-[4-methyl-5-(2-phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-thiazol-2-yl]-amine(85545-47-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 85545-47-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85545-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,4 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85545-47:
(7*8)+(6*5)+(5*5)+(4*4)+(3*5)+(2*4)+(1*7)=157
157 % 10 = 7
So 85545-47-7 is a valid CAS Registry Number.

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85545-47-7Relevant academic research and scientific papers

Synthesis and Biological Activity of Some New 1,5-Benzothiazepines Containing Thiazole Moiety - 2-Aryl-4-(4'-methyl-2'-disubstituted-aminothiazol-5'-yl)-2,3-dihydro-1,5-benzothiazepines

Mane, R. A.,Ingle, D. B.

, p. 973 - 974 (2007/10/02)

The title compounds (III) have been synthesized from the corresponding 5--4-methyl-2-substituted-aminothiazoles (II) by condensation with o-aminothiophenol (I) in refluxing ethanol containing a few drops of piperidine, followed by cyclisation in the presence of acetic acid.Some of the compounds show antifungal and antibacterial activities.

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