Cas 25919-83-9,<i>N</i>-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-3-methyl-butyramide

25919-83-9

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Basic information

Product Name: N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-3-methyl-butyramide
Synonyms: N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-3-methyl-butyramide
CAS NO:25919-83-9
Molecular Formula:
Molecular Weight: 434.603
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: N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-3-methyl-butyramide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-3-methyl-butyramide(25919-83-9)
EPA Substance Registry System: N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-3-methyl-butyramide(25919-83-9)

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: 25919-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 25919-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,1 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25919-83:
(7*2)+(6*5)+(5*9)+(4*1)+(3*9)+(2*8)+(1*3)=139
139 % 10 = 9
So 25919-83-9 is a valid CAS Registry Number.

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25919-83-9Relevant 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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