Cas 1027261-86-4,3-Oxo-2-[1-(2-phenyl-3H-imidazol-4-yl)-meth-(Z)-ylidene]-butyric acid 3-cyclohexyl-propyl ester

1027261-86-4

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Basic information

Product Name: 3-Oxo-2-[1-(2-phenyl-3H-imidazol-4-yl)-meth-(Z)-ylidene]-butyric acid 3-cyclohexyl-propyl ester
Synonyms:
CAS NO:1027261-86-4
Molecular Formula:
Molecular Weight: 380.487
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: 3-Oxo-2-[1-(2-phenyl-3H-imidazol-4-yl)-meth-(Z)-ylidene]-butyric acid 3-cyclohexyl-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Oxo-2-[1-(2-phenyl-3H-imidazol-4-yl)-meth-(Z)-ylidene]-butyric acid 3-cyclohexyl-propyl ester(1027261-86-4)
EPA Substance Registry System: 3-Oxo-2-[1-(2-phenyl-3H-imidazol-4-yl)-meth-(Z)-ylidene]-butyric acid 3-cyclohexyl-propyl ester(1027261-86-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1027261-86-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027261-86-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,2,6 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1027261-86:
(9*1)+(8*0)+(7*2)+(6*7)+(5*2)+(4*6)+(3*1)+(2*8)+(1*6)=124
124 % 10 = 4
So 1027261-86-4 is a valid CAS Registry Number.

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1027261-86-4Relevant academic research and scientific papers

Synthesis and calcium channel antagonist activity of new 1,4-dihydropyridine derivatives containing lipophilic 4-imidazolyl substituents

Navidpour, Latifeh,Miri, Ramin,Shafiee, Abbas

, p. 499 - 504 (2007/10/03)

A group of cycloalkyl and aryl ester analogues of nifedipine (CAS 21829-25-4), in which the ortho-nitrophenyl group at position 4 is replaced by a 2-phenyl-4(5)-imidazolyl substituent, were synthesized and evaluated as calcium channel antagonist using the

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