Cas 5285-98-3,3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carbonitrile

5285-98-3

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Basic information

Product Name: 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carbonitrile
Synonyms: 3-Amino-4,6-dimethylthieno[2,3-b]pyridine-2-carbonitrile; Thieno[2,3-b]pyridine-2-carbonitrile, 3-amino-4,6-dimethyl-
CAS NO:5285-98-3
Molecular Formula: C₁₀H₁₁NOS
Molecular Weight: 203.2636
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 419.6°C at 760 mmHg
Flash Point: 207.5°C
Appearance: N/A
Density: 1.33g/cm³
Vapor Pressure: 3.01E-07mmHg at 25°C
Refractive Index: 1.68
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carbonitrile(5285-98-3)
EPA Substance Registry System: 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carbonitrile(5285-98-3)

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: 5285-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 5285-98-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5285-98:
(6*5)+(5*2)+(4*8)+(3*5)+(2*9)+(1*8)=113
113 % 10 = 3
So 5285-98-3 is a valid CAS Registry Number.

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5285-98-3Downstream Products

5285-98-3Relevant academic research and scientific papers

Electrochemical ipso-Thiocyanation of Arylboron Compounds

Dyga, Marco,Hayrapetyan, Davit,Rit, Raja K.,Goo?en, Lukas J.

supporting information, p. 3548 - 3553 (2019/04/26)

An operationally simple electrochemical method for the transition-metal-free ipso-thiocyanation of arylboronic acids and aryl trifluoroborates has been developed. The SCN electrophile is generated in situ by anodic oxidation of thiocyanate anions, which avoids formation of salt waste and prevents unwanted side reactions arising from chemical oxidants. The reaction proceeds regiospecifically, and the scope extends to non-activated aromatic systems. (Figure presented.).

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