Cas 1078164-06-3,2-amino-4-(4-methoxyphenyl)-5-(2-methylpropyl)-6-(methylsulfinyl)pyridine-3-carbonitrile

1078164-06-3

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Basic information

Product Name: 2-amino-4-(4-methoxyphenyl)-5-(2-methylpropyl)-6-(methylsulfinyl)pyridine-3-carbonitrile
Synonyms: 2-amino-4-(4-methoxyphenyl)-5-(2-methylpropyl)-6-(methylsulfinyl)pyridine-3-carbonitrile
CAS NO:1078164-06-3
Molecular Formula:
Molecular Weight: 343.45
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: 2-amino-4-(4-methoxyphenyl)-5-(2-methylpropyl)-6-(methylsulfinyl)pyridine-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-4-(4-methoxyphenyl)-5-(2-methylpropyl)-6-(methylsulfinyl)pyridine-3-carbonitrile(1078164-06-3)
EPA Substance Registry System: 2-amino-4-(4-methoxyphenyl)-5-(2-methylpropyl)-6-(methylsulfinyl)pyridine-3-carbonitrile(1078164-06-3)

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: 1078164-06-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1078164-06-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,8,1,6 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1078164-06:
(9*1)+(8*0)+(7*7)+(6*8)+(5*1)+(4*6)+(3*4)+(2*0)+(1*6)=153
153 % 10 = 3
So 1078164-06-3 is a valid CAS Registry Number.

1078164-06-3Upstream product

1078164-02-9 2-amino-4-(4-methoxyphenyl)-5-(2-methylpropyl)-6-(methylsulfanyl)pyridine-3-carbonitrile

1078164-06-3Downstream Products

1078164-06-3Relevant academic research and scientific papers

Synthesis of heavily substituted 2-aminopyridines by displacement of a 6-methylsulfinyl group

Teague, Simon J.

, p. 9765 - 9766 (2008)

(Chemical Equation Presented) 2-Aminopyridines, with a variety of polar 6-substituents, were elaborated by displacement of a methylsulfinyl group from the 6-position of the pyridine ring. The requisite 6-thiomethyl pyridines were synthesized by reaction o

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