Cas 138989-93-2,(E)-N-[(1R,2R)-2-(2,4-Difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-3-(4-trifluoromethoxy-phenyl)-acrylamide

138989-93-2

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Basic information

Product Name: (E)-N-[(1R,2R)-2-(2,4-Difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-3-(4-trifluoromethoxy-phenyl)-acrylamide
Synonyms:
CAS NO:138989-93-2
Molecular Formula:
Molecular Weight: 482.41
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: (E)-N-[(1R,2R)-2-(2,4-Difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-3-(4-trifluoromethoxy-phenyl)-acrylamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-N-[(1R,2R)-2-(2,4-Difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-3-(4-trifluoromethoxy-phenyl)-acrylamide(138989-93-2)
EPA Substance Registry System: (E)-N-[(1R,2R)-2-(2,4-Difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-3-(4-trifluoromethoxy-phenyl)-acrylamide(138989-93-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 138989-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138989-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,8 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138989-93:
(8*1)+(7*3)+(6*8)+(5*9)+(4*8)+(3*9)+(2*9)+(1*3)=202
202 % 10 = 2
So 138989-93-2 is a valid CAS Registry Number.

138989-93-2Upstream product

126917-48-4 (2R,3R)-3-Azido-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol

138989-93-2Downstream Products

138989-93-2Relevant academic research and scientific papers

Triazole antifungals. IV. Synthesis and antifungal activities of 3-acylamino-2-aryl-2-butanol derivatives

Konosu,Tajima,Takeda,Miyaoka,Kasahara,Yasuda,Oida

, p. 2581 - 2589 (2007/10/02)

New triazole compounds were designed and synthesized as potential inhibitors of the fungal cytochrome P-450 14α-demethylase. In testing for antifungal activity against a mouse systemic Candida albicans infection, (2R,3R)3-acylamino-2-aryl-2-butanol deriva

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