Cas 36047-61-7,5-(2-phenylethyl)-5H-[1,2,4]triazino[5,6-b]indol-3-yl hydrosulfide

36047-61-7

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Basic information

Product Name: 5-(2-phenylethyl)-5H-[1,2,4]triazino[5,6-b]indol-3-yl hydrosulfide
Synonyms: 5-(2-phenylethyl)-5H-[1,2,4]triazino[5,6-b]indol-3-yl hydrosulfide
CAS NO:36047-61-7
Molecular Formula: C₁₇H₁₄N₄S
Molecular Weight: 306.38486
EINECS: N/A
Product Categories: N/A
Mol File: 36047-61-7.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: 5-(2-phenylethyl)-5H-[1,2,4]triazino[5,6-b]indol-3-yl hydrosulfide(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2-phenylethyl)-5H-[1,2,4]triazino[5,6-b]indol-3-yl hydrosulfide(36047-61-7)
EPA Substance Registry System: 5-(2-phenylethyl)-5H-[1,2,4]triazino[5,6-b]indol-3-yl hydrosulfide(36047-61-7)

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: 36047-61-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 36047-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,4 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36047-61:
(7*3)+(6*6)+(5*0)+(4*4)+(3*7)+(2*6)+(1*1)=107
107 % 10 = 7
So 36047-61-7 is a valid CAS Registry Number.

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36047-61-7Relevant academic research and scientific papers

Synthesis of hetarylsulfanyl- and hetaryloxyfuroxans by nucleophilic substitution of nitro group in nitrofuroxans with heterocyclic thiol and hydroxy derivatives

Fershtat, Leonid L.,Epishina, Margarita A.,Kulikov, Alexander S.,Struchkova, Marina I.,Makhova, Nina N.

, p. 176 - 186 (2015)

[Figure not available: see fulltext.] We report a general method for the synthesis of previously unknown heterocyclic systems containing furoxan and heterocyclic fragments linked by S- and O-bridges, based on nucleophilic substitution of nitro group in 4-

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