Cas 556824-96-5,N-[4-(dimethylamino)phenyl]-N-[3-(4-phenyl-1,3-thiazol-2-yl)-2H-chromen-2-ylidene]amine

556824-96-5

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Basic information

Product Name: N-[4-(dimethylamino)phenyl]-N-[3-(4-phenyl-1,3-thiazol-2-yl)-2H-chromen-2-ylidene]amine
Synonyms: N-[4-(dimethylamino)phenyl]-N-[3-(4-phenyl-1,3-thiazol-2-yl)-2H-chromen-2-ylidene]amine
CAS NO:556824-96-5
Molecular Formula: C26H21N3OS
Molecular Weight: 423.52944
EINECS: N/A
Product Categories: N/A
Mol File: 556824-96-5.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: N-[4-(dimethylamino)phenyl]-N-[3-(4-phenyl-1,3-thiazol-2-yl)-2H-chromen-2-ylidene]amine(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-(dimethylamino)phenyl]-N-[3-(4-phenyl-1,3-thiazol-2-yl)-2H-chromen-2-ylidene]amine(556824-96-5)
EPA Substance Registry System: N-[4-(dimethylamino)phenyl]-N-[3-(4-phenyl-1,3-thiazol-2-yl)-2H-chromen-2-ylidene]amine(556824-96-5)

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: 556824-96-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 556824-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,8,2 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 556824-96:
(8*5)+(7*5)+(6*6)+(5*8)+(4*2)+(3*4)+(2*9)+(1*6)=195
195 % 10 = 5
So 556824-96-5 is a valid CAS Registry Number.

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556824-96-5Relevant academic research and scientific papers

Reactions of 3-(4-aryl-2-thiazolyl)- and 3-(2-benzothiazolyl)-2-iminocoumarins with N-nucleophiles

Gorobets,Borisov,Silin,Nikitchenko,Kovalenko

, p. 1389 - 1396 (2007/10/03)

The reaction of 3-(4-aryl-2-thiazolyl)- and 3-(2-benzothiazolyl)-2-iminocoumarins with N-nucleophiles was studied. This reaction gives 2-N-substituted 3-(4-aryl-2-thiazolyl)- and 3-(2-benzothiazolyl)-iminocourmarins. N-Nucleophiles such as arylamines, het

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