Cas 170573-91-8,1H-1,2,4-Triazole, 1-[[2-(2,4-difluorophenyl)-3,3-dimethyl-1,4-oxathian-2-yl]methyl]-

170573-91-8

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Basic information

Product Name: 1H-1,2,4-Triazole, 1-[[2-(2,4-difluorophenyl)-3,3-dimethyl-1,4-oxathian-2-yl]methyl]-
Synonyms:
CAS NO:170573-91-8
Molecular Formula: C15H17F2N3OS
Molecular Weight: 325.382
EINECS: N/A
Product Categories: N/A
Mol File: 170573-91-8.mol

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: 1H-1,2,4-Triazole, 1-[[2-(2,4-difluorophenyl)-3,3-dimethyl-1,4-oxathian-2-yl]methyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-1,2,4-Triazole, 1-[[2-(2,4-difluorophenyl)-3,3-dimethyl-1,4-oxathian-2-yl]methyl]-(170573-91-8)
EPA Substance Registry System: 1H-1,2,4-Triazole, 1-[[2-(2,4-difluorophenyl)-3,3-dimethyl-1,4-oxathian-2-yl]methyl]-(170573-91-8)

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: 170573-91-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 170573-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,5,7 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 170573-91:
(8*1)+(7*7)+(6*0)+(5*5)+(4*7)+(3*3)+(2*9)+(1*1)=138
138 % 10 = 8
So 170573-91-8 is a valid CAS Registry Number.

170573-91-8Upstream product

167214-29-1 2-(2,4-Difluoro-phenyl)-3-(2-hydroxy-ethylsulfanyl)-3-methyl-1-[1,2,4]triazol-1-yl-butan-2-ol

170573-91-8Downstream Products

170573-91-8Relevant academic research and scientific papers

Synthesis and antifungal activity of new azole derivatives containing an oxathiane ring

Miyauchi, Hiroshi,Tanio, Tomoharu,Ohashi, Naohito

, p. 2377 - 2380 (1996)

A series of azole derivatives containing an oxathiane ring, which were designed to simulate the D ring of lanosterol, were synthesized and evaluated for their antifungal activity. 3,3-Dimethyl derivatives showed potent activity against murine systemic candidosis and aspergillosis, whereas (2R*,3R*)-3-monomethyl derivatives showed only weak activity in both in vitro and in vivo.

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