Cas 91510-04-2,(2R<sup>*</sup>,3R<sup>*</sup>)-2-(2,4-dichlorophenyl)-3-carbamoyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol

91510-04-2

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Basic information

Product Name: (2R^*,3R^*)-2-(2,4-dichlorophenyl)-3-carbamoyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol
Synonyms:
CAS NO:91510-04-2
Molecular Formula:
Molecular Weight: 329.186
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: (2R^*,3R^*)-2-(2,4-dichlorophenyl)-3-carbamoyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol(CAS DataBase Reference)
NIST Chemistry Reference: (2R^*,3R^*)-2-(2,4-dichlorophenyl)-3-carbamoyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol(91510-04-2)
EPA Substance Registry System: (2R^*,3R^*)-2-(2,4-dichlorophenyl)-3-carbamoyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol(91510-04-2)

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: 91510-04-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91510-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91510-04:
(7*9)+(6*1)+(5*5)+(4*1)+(3*0)+(2*0)+(1*4)=102
102 % 10 = 2
So 91510-04-2 is a valid CAS Registry Number.

91510-04-2Upstream product

91510-26-8 (2R^*,3R^*)-2-(2,4-dichlorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butyric acid

91510-04-2Downstream Products

91510-04-2Relevant academic research and scientific papers

Triazole antifungals. V. Synthesis and antifungal activities of some amides related to 3-acylamino-2-aryl-1-triazolyl-2-butanol

Tanaka,Takeda,Konosu,Yasuda,Oida

, p. 661 - 665 (1992)

Amides, 2 and 3, related to the potent antifungal triazole-amide 3-acylamino-2-aryl-1-triazolyl-2-butanol (1) were synthesized starting from the triazole-alcohol 6. The antifungal activity of 2 and 3 against a mouse systemic Candida albicans infection was

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