Cas 120187-03-3,6-(4-nitrophenyl)-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole

120187-03-3

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Basic information

Product Name: 6-(4-nitrophenyl)-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole
Synonyms: 6-(4-nitrophenyl)-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole
CAS NO:120187-03-3
Molecular Formula:
Molecular Weight: 353.361
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: 6-(4-nitrophenyl)-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole(CAS DataBase Reference)
NIST Chemistry Reference: 6-(4-nitrophenyl)-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole(120187-03-3)
EPA Substance Registry System: 6-(4-nitrophenyl)-3-(4-methoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole(120187-03-3)

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: 120187-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120187-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,8 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120187-03:
(8*1)+(7*2)+(6*0)+(5*1)+(4*8)+(3*7)+(2*0)+(1*3)=83
83 % 10 = 3
So 120187-03-3 is a valid CAS Registry Number.

120187-03-3Upstream product

120187-03-3Downstream Products

120187-03-3Relevant academic research and scientific papers

Unprecedented conversion of (Z)-3-chloro-3-arylacrylic acids to benzoic acids: Synthesis of s-triazolo[3,4-b][1,3,4]thiadiazoles

Sahi, Seema,Bhardwaj, Madhvi,Paul, Satya

, p. 3809 - 3812 (2014)

An unprecedented method for the conversion of (Z)-3-chloro-3-arylacrylic acids to corresponding benzoic acids by stirring in POCl3 at 80 °C is reported. The benzoic acids formed in situ undergo condensation with 4-amino-5-aryl-3-mercapto-1,2,4-

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