Cas 140845-75-6,3,5-Pyridinedicarboxylic acid, 4-(4-bromophenyl)-1,4-dihydro-1-phenyl-2,6-bis(thiocyanatomethyl)-, diethyl ester

140845-75-6

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Basic information

Product Name: 3,5-Pyridinedicarboxylic acid, 4-(4-bromophenyl)-1,4-dihydro-1-phenyl-2,6-bis(thiocyanatomethyl)-, diethyl ester
Synonyms:
CAS NO:140845-75-6
Molecular Formula: C27H24BrN3O4S2
Molecular Weight: 598.541
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-Pyridinedicarboxylic acid, 4-(4-bromophenyl)-1,4-dihydro-1-phenyl-2,6-bis(thiocyanatomethyl)-, diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3,5-Pyridinedicarboxylic acid, 4-(4-bromophenyl)-1,4-dihydro-1-phenyl-2,6-bis(thiocyanatomethyl)-, diethyl ester(140845-75-6)
EPA Substance Registry System: 3,5-Pyridinedicarboxylic acid, 4-(4-bromophenyl)-1,4-dihydro-1-phenyl-2,6-bis(thiocyanatomethyl)-, diethyl ester(140845-75-6)

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: 140845-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140845-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,4 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 140845-75:
(8*1)+(7*4)+(6*0)+(5*8)+(4*4)+(3*5)+(2*7)+(1*5)=126
126 % 10 = 6
So 140845-75-6 is a valid CAS Registry Number.

140845-75-6Upstream product

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140845-75-6Relevant academic research and scientific papers

BROMINATION OF 4-ARYL-3,5-DIALKOXYCARBONYL-2,6-DIMETHYL-1,4-DIHYDROPYRIDINES

Skrastin'sh, I. P.,Kastron, V. V.,Chekavichus, B. S.,Sausin'sh, A. E.,Zolotoyabko, R. M.,Dubur, G. Ya.

, p. 989 - 994 (2007/10/02)

4-Aryl-3,5-dialkoxycarbonyl-2,6-dimethyl-1,4-dihydropyridines are brominated by N-bromosuccinimide in methanol at room temperature at the methyl groups at positions 2 and 6 to form mono-, di-, tri-, and tetrabromo derivatives.When the N-unsubstituted brom

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