Cas 1623097-82-4,5H-3-(phenacylthio)-7-methoxy[1,2,4]triazino[5,6-b]indole hydrobromide

1623097-82-4

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Basic information

Product Name: 5H-3-(phenacylthio)-7-methoxy[1,2,4]triazino[5,6-b]indole hydrobromide
Synonyms: 5H-3-(phenacylthio)-7-methoxy[1,2,4]triazino[5,6-b]indole hydrobromide
CAS NO:1623097-82-4
Molecular Formula:
Molecular Weight: 431.313
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: 5H-3-(phenacylthio)-7-methoxy[1,2,4]triazino[5,6-b]indole hydrobromide(CAS DataBase Reference)
NIST Chemistry Reference: 5H-3-(phenacylthio)-7-methoxy[1,2,4]triazino[5,6-b]indole hydrobromide(1623097-82-4)
EPA Substance Registry System: 5H-3-(phenacylthio)-7-methoxy[1,2,4]triazino[5,6-b]indole hydrobromide(1623097-82-4)

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: 1623097-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1623097-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,3,0,9 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1623097-82:
(9*1)+(8*6)+(7*2)+(6*3)+(5*0)+(4*9)+(3*7)+(2*8)+(1*2)=164
164 % 10 = 4
So 1623097-82-4 is a valid CAS Registry Number.

1623097-82-4Upstream product

1623097-82-4Downstream Products

1623097-85-7 3-(phenyl)-8-methoxythiazolo[3',2':2,3][1,2,4]triazino[5,6-b]indole

1623097-82-4Relevant academic research and scientific papers

A multistep preparation of 3-Aryl-8-methoxythiazolo [3′,2′:2,3] [1,2,4] triazino [5,6-b] indoles under microwave IR-radiations

Singh, Ravinder

, p. 319 - 323 (2014/06/23)

The different 3-Aryl-8-methoxythiazolo [3′,2′:2,3] [1,2,4] triazino [5,6-b] Indoles having antihistaminc, antithyroid, antitubercular, antifungal & antibacterial activities are synthesized through a multistep preparation in high yield in shorter reaction

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