Cas 438231-54-0,5-(2-methyl-3-furyl)-4-(2-methylphenyl)-4H-1,2,4-triazol-3-yl hydrosulfide

438231-54-0

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Basic information

Product Name: 5-(2-methyl-3-furyl)-4-(2-methylphenyl)-4H-1,2,4-triazol-3-yl hydrosulfide
Synonyms: 5-(2-methyl-3-furyl)-4-(2-methylphenyl)-4H-1,2,4-triazol-3-yl hydrosulfide
CAS NO:438231-54-0
Molecular Formula: C₁₄H₁₃N₃OS
Molecular Weight: 271.33752
EINECS: N/A
Product Categories: N/A
Mol File: 438231-54-0.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-methyl-3-furyl)-4-(2-methylphenyl)-4H-1,2,4-triazol-3-yl hydrosulfide(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2-methyl-3-furyl)-4-(2-methylphenyl)-4H-1,2,4-triazol-3-yl hydrosulfide(438231-54-0)
EPA Substance Registry System: 5-(2-methyl-3-furyl)-4-(2-methylphenyl)-4H-1,2,4-triazol-3-yl hydrosulfide(438231-54-0)

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: 438231-54-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 438231-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,2,3 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 438231-54:
(8*4)+(7*3)+(6*8)+(5*2)+(4*3)+(3*1)+(2*5)+(1*4)=140
140 % 10 = 0
So 438231-54-0 is a valid CAS Registry Number.

438231-54-0Upstream product

438232-76-9 C₁₄H₁₅N₃O₂S

438231-54-0Downstream Products

438231-54-0Relevant academic research and scientific papers

Antimicrobial properties of 4-Aryl-3-(2-methyl-furan-3-yl) δ2-1,2,4-triazoline-5-thiones

Siwek, Agata,Wujec, Monika,Stefanska, Joanna,Paneth, Piotr

scheme or table, p. 3149 - 3159 (2010/04/26)

Four 4-aryl-3-(2-methyl-furan-3-yl)- δ2-1,2,4-triazole-5- thiones were synthesized by intramolecular cyclization of 4-aryl-1-[(2-methyl- furan-3-yl)carbonyl]thiosemicarbazides in alkaline medium. The antimicrobial activity of the synthesized tr

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