Cas 1263308-25-3,3,5-diamino-4-cyano-N'-[1-(4-(piperidin-1-ylsulfonyl)phenyl)ethylidene]thiophene-2-carbohydrazide

1263308-25-3

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Basic information

Product Name: 3,5-diamino-4-cyano-N'-[1-(4-(piperidin-1-ylsulfonyl)phenyl)ethylidene]thiophene-2-carbohydrazide
Synonyms: 3,5-diamino-4-cyano-N'-[1-(4-(piperidin-1-ylsulfonyl)phenyl)ethylidene]thiophene-2-carbohydrazide
CAS NO:1263308-25-3
Molecular Formula:
Molecular Weight: 446.554
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: 3,5-diamino-4-cyano-N'-[1-(4-(piperidin-1-ylsulfonyl)phenyl)ethylidene]thiophene-2-carbohydrazide(CAS DataBase Reference)
NIST Chemistry Reference: 3,5-diamino-4-cyano-N'-[1-(4-(piperidin-1-ylsulfonyl)phenyl)ethylidene]thiophene-2-carbohydrazide(1263308-25-3)
EPA Substance Registry System: 3,5-diamino-4-cyano-N'-[1-(4-(piperidin-1-ylsulfonyl)phenyl)ethylidene]thiophene-2-carbohydrazide(1263308-25-3)

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: 1263308-25-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1263308-25-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,3,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1263308-25:
(9*1)+(8*2)+(7*6)+(6*3)+(5*3)+(4*0)+(3*8)+(2*2)+(1*5)=133
133 % 10 = 3
So 1263308-25-3 is a valid CAS Registry Number.

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1263308-25-3Relevant academic research and scientific papers

Anti-breast cancer activity of some novel 1,2-dihydropyridine, thiophene and thiazole derivatives

Al-Said, Mansour S.,Bashandy, Mahmoud S.,Al-Qasoumi, Saleh I.,Ghorab, Mostafa M.

experimental part, p. 137 - 141 (2011/02/27)

A variety of novel 1,2-dihydropyridines 10-17, thiophenes 18-21 and thiazole 22 having a biologically active sulfone moiety were obtained via the reaction of 2-cyano-N′-[1-(4-(piperidin-1-ylsulfonyl) phenyl) ethylidene] acetohydrazide 3 with a variety of

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