Cas 354784-23-9,2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile

354784-23-9

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Basic information

Product Name: 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile
Synonyms: 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile
CAS NO:354784-23-9
Molecular Formula: C₁₆H₁₁N₅OS
Molecular Weight: 321.35644
EINECS: N/A
Product Categories: N/A
Mol File: 354784-23-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile(354784-23-9)
EPA Substance Registry System: 2-amino-6-[(cyanomethyl)sulfanyl]-4-(4-methoxyphenyl)-3,5-pyridinedicarbonitrile(354784-23-9)

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: 354784-23-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 354784-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,7,8 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 354784-23:
(8*3)+(7*5)+(6*4)+(5*7)+(4*8)+(3*4)+(2*2)+(1*3)=169
169 % 10 = 9
So 354784-23-9 is a valid CAS Registry Number.

354784-23-9Upstream product

354784-23-9Downstream Products

476319-02-5 3,6-diamino-4-(4-methoxyphenyl)thieno[2,3-b]pyridine-2,5-dicarbonitrile

354784-23-9Relevant academic research and scientific papers

Keactions with 3,6-diaminothieno[2,3-b]-pyridines: Synthesis and characterization of several new fused pyridine heterocycles

Gad-Elkareem, Mohamed A. M.,Elneairy, Mohamed A. A.,Taha, Adel M.

, p. 405 - 413 (2008/02/12)

6-Aminopyridine-2(1H)thiones 1 reacting with a-halo-compounds 2a-c afforded the alkylthiopyridine derivatives 3a-c which in turn cyclized to the corresponding thieno[2,3-b]pyridine derivatives 4a-c. Several thieno[2,3-b]pyridine derivatives 7, 16, 19, pyr

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