Cas 442670-70-4,3-(4-fluorophenyl)-6-methyl-1,2,4-triazolo[3,4-b][2H-1,3,4]thiadiazine

442670-70-4

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Basic information

Product Name: 3-(4-fluorophenyl)-6-methyl-1,2,4-triazolo[3,4-b][2H-1,3,4]thiadiazine
Synonyms: 3-(4-fluorophenyl)-6-methyl-1,2,4-triazolo[3,4-b][2H-1,3,4]thiadiazine
CAS NO:442670-70-4
Molecular Formula:
Molecular Weight: 248.284
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: 3-(4-fluorophenyl)-6-methyl-1,2,4-triazolo[3,4-b][2H-1,3,4]thiadiazine(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-fluorophenyl)-6-methyl-1,2,4-triazolo[3,4-b][2H-1,3,4]thiadiazine(442670-70-4)
EPA Substance Registry System: 3-(4-fluorophenyl)-6-methyl-1,2,4-triazolo[3,4-b][2H-1,3,4]thiadiazine(442670-70-4)

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: 442670-70-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 442670-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,2,6,7 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 442670-70:
(8*4)+(7*4)+(6*2)+(5*6)+(4*7)+(3*0)+(2*7)+(1*0)=144
144 % 10 = 4
So 442670-70-4 is a valid CAS Registry Number.

442670-70-4Upstream product

442670-70-4Downstream Products

442670-70-4Relevant academic research and scientific papers

Synthesis of imidazo[2,1-b][2H-1,3,4]thiadiazines and 1,2,4-triazolo[3,4-b][2H-1,3,4]thiadiazines

Knak, Stefanie,Pfeiffer, Wolf-Diethard,Dollinger, Horst,Saghyan, Ashot S.,Langer, Peter

, p. 463 - 467 (2015)

Imidazo[2,1-b][2H-1,3,4]thiadiazines were prepared by cyclization of 2-amino-5-(4-chlorophenyl)-6H-1,3,4-thiadiazine with α-haloketones. 1,2,4-Triazolo[3,4-b][2H-1,3,4]thiadiazines were prepared by cyclization of 4-amino-5-sulfanyl-l,2,4-triazoles with ph

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