Cas 126917-75-7,Naphthalene-2-carboxylic acid [(1S,2S)-2-(2,4-difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-amide

126917-75-7

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Basic information

Product Name: Naphthalene-2-carboxylic acid [(1S,2S)-2-(2,4-difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-amide
Synonyms:
CAS NO:126917-75-7
Molecular Formula:
Molecular Weight: 422.434
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: Naphthalene-2-carboxylic acid [(1S,2S)-2-(2,4-difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-amide(CAS DataBase Reference)
NIST Chemistry Reference: Naphthalene-2-carboxylic acid [(1S,2S)-2-(2,4-difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-amide(126917-75-7)
EPA Substance Registry System: Naphthalene-2-carboxylic acid [(1S,2S)-2-(2,4-difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl]-amide(126917-75-7)

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: 126917-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126917-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,1 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126917-75:
(8*1)+(7*2)+(6*6)+(5*9)+(4*1)+(3*7)+(2*7)+(1*5)=147
147 % 10 = 7
So 126917-75-7 is a valid CAS Registry Number.

126917-75-7Upstream product

126917-75-7Downstream Products

126917-75-7Relevant 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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