Cas 25921-68-0,5-chloro-<i>N</i>-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-2-methoxy-benzamide

25921-68-0

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Basic information

Product Name: 5-chloro-N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-2-methoxy-benzamide
Synonyms: 5-chloro-N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-2-methoxy-benzamide
CAS NO:25921-68-0
Molecular Formula:
Molecular Weight: 519.065
EINECS: N/A
Product Categories: N/A
Mol File: 25921-68-0.mol
Article Data: 1

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: 5-chloro-N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-2-methoxy-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 5-chloro-N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-2-methoxy-benzamide(25921-68-0)
EPA Substance Registry System: 5-chloro-N-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethyl]-2-methoxy-benzamide(25921-68-0)

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: 25921-68-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 25921-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,2 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25921-68:
(7*2)+(6*5)+(5*9)+(4*2)+(3*1)+(2*6)+(1*8)=120
120 % 10 = 0
So 25921-68-0 is a valid CAS Registry Number.

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25921-68-0Relevant articles and documents

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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