Cas 208254-37-9,2-{[6-amino-4-(4-bromophenyl)-3,5-dicyano-2-pyridinyl]sulfanyl}-N-(4-bromophenyl)acetamide

208254-37-9

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Basic information

Product Name: 2-{[6-amino-4-(4-bromophenyl)-3,5-dicyano-2-pyridinyl]sulfanyl}-N-(4-bromophenyl)acetamide
Synonyms: 2-{[6-amino-4-(4-bromophenyl)-3,5-dicyano-2-pyridinyl]sulfanyl}-N-(4-bromophenyl)acetamide
CAS NO:208254-37-9
Molecular Formula: C21H13Br2N5OS
Molecular Weight: 543.23382
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 758.6±60.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.80±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 11.92±0.70(Predicted)
CAS DataBase Reference: 2-{[6-amino-4-(4-bromophenyl)-3,5-dicyano-2-pyridinyl]sulfanyl}-N-(4-bromophenyl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-{[6-amino-4-(4-bromophenyl)-3,5-dicyano-2-pyridinyl]sulfanyl}-N-(4-bromophenyl)acetamide(208254-37-9)
EPA Substance Registry System: 2-{[6-amino-4-(4-bromophenyl)-3,5-dicyano-2-pyridinyl]sulfanyl}-N-(4-bromophenyl)acetamide(208254-37-9)

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: 208254-37-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 208254-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,2,5 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 208254-37:
(8*2)+(7*0)+(6*8)+(5*2)+(4*5)+(3*4)+(2*3)+(1*7)=119
119 % 10 = 9
So 208254-37-9 is a valid CAS Registry Number.

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208254-37-9Relevant academic research and scientific papers

New Route to 6-Amino-4-aryl-3,5-dicyano-pyridine-2(1H)-thiones

Dyachenko,Krivokolysko,Sharanin,Litvinov

, p. 1014 - 1017 (2007/10/03)

Condensation of aromatic aldehydes with a twofold amount of cyanothioacetamide yields 6-amino-4-aryl-3,5-dicyanopyridine-2(1H)-thiones. These compounds are also formed by recyclization of 2,6-diamino-4-aryl-3,5-dicyano-4H-thiopyrans. 6-Amino-4-aryl-3,5-dicyanopyridine-2(1H)-thiones were used to prepare substituted 2-alkylthiopyridines and thieno[2,3-6]pyridines.

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