Cas 34958-25-3,1-cyclohexyl-3-{4-[2-(3,4-dichloro-benzoylamino)-ethyl]-benzenesulfonyl}-imidazolidin-2-ylideneamine

34958-25-3

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Basic information

Product Name: 1-cyclohexyl-3-{4-[2-(3,4-dichloro-benzoylamino)-ethyl]-benzenesulfonyl}-imidazolidin-2-ylideneamine
Synonyms: 1-cyclohexyl-3-{4-[2-(3,4-dichloro-benzoylamino)-ethyl]-benzenesulfonyl}-imidazolidin-2-ylideneamine
CAS NO:34958-25-3
Molecular Formula:
Molecular Weight: 523.483
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-cyclohexyl-3-{4-[2-(3,4-dichloro-benzoylamino)-ethyl]-benzenesulfonyl}-imidazolidin-2-ylideneamine(CAS DataBase Reference)
NIST Chemistry Reference: 1-cyclohexyl-3-{4-[2-(3,4-dichloro-benzoylamino)-ethyl]-benzenesulfonyl}-imidazolidin-2-ylideneamine(34958-25-3)
EPA Substance Registry System: 1-cyclohexyl-3-{4-[2-(3,4-dichloro-benzoylamino)-ethyl]-benzenesulfonyl}-imidazolidin-2-ylideneamine(34958-25-3)

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: 34958-25-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 34958-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,5 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34958-25:
(7*3)+(6*4)+(5*9)+(4*5)+(3*8)+(2*2)+(1*5)=143
143 % 10 = 3
So 34958-25-3 is a valid CAS Registry Number.

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34958-25-3Relevant 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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