Cas 25865-17-2,1-methyl-cyclohex-3-enecarboxylic acid 4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethylamide

25865-17-2

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Basic information

Product Name: 1-methyl-cyclohex-3-enecarboxylic acid 4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethylamide
Synonyms:
CAS NO:25865-17-2
Molecular Formula:
Molecular Weight: 472.652
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: 1-methyl-cyclohex-3-enecarboxylic acid 4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethylamide(CAS DataBase Reference)
NIST Chemistry Reference: 1-methyl-cyclohex-3-enecarboxylic acid 4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethylamide(25865-17-2)
EPA Substance Registry System: 1-methyl-cyclohex-3-enecarboxylic acid 4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethylamide(25865-17-2)

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: 25865-17-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 25865-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,6 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25865-17:
(7*2)+(6*5)+(5*8)+(4*6)+(3*5)+(2*1)+(1*7)=132
132 % 10 = 2
So 25865-17-2 is a valid CAS Registry Number.

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25865-17-2Relevant academic research and scientific papers

Sulfonyliminoimidazolidines. A new class of oral hypoglycemic agents. I. 1-[[p-[2-(Acylamino)ethyl]phenyl]sulfonyl]-2-iminoimidazolidines

Schweizer,Marki,Lehmann,Dietrich

, p. 964 - 970 (2007/10/02)

A series of 1-[[p-[2-(acylamino)ethyl]phenyl]sulfonyl]-2-iminoimidazolidines has been synthesized. Compounds from this new class of oral hypoglycemic agents lower blood glucose in normal and in streptozotocin-diabetic rats. Potent analogues were obtained

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