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171764-49-1

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171764-49-1 Usage

General Description

The chemical "(2R,4R) CIS-(2,4-DIFLUOROPHENYL)-2-(1,2,4-TRIAZOLE-1-YL-METHYL)-1,3-DIOXOLANE-4YL-METHYL-P-TOLYSULFONATE" is a compound containing a dioxolane ring with a 1,2,4-triazole-1-yl-methyl group attached. It also includes a p-tolylsulfonate moiety. The compound is a sulfonate ester derived from p-toluenesulfonic acid, while the rest of the molecule consists of a combination of fluoro-substituted phenyl and 1,2,4-triazole groups. This chemical has potential applications in pharmaceuticals, agrochemicals, and materials science, given its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 171764-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,7,6 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 171764-49:
(8*1)+(7*7)+(6*1)+(5*7)+(4*6)+(3*4)+(2*4)+(1*9)=151
151 % 10 = 1
So 171764-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H21F2N3O4S/c1-15-2-5-18(6-3-15)31(27,28)9-8-17-11-29-21(30-17,12-26-14-24-13-25-26)19-7-4-16(22)10-20(19)23/h2-7,10,13-14,17H,8-9,11-12H2,1H3/t17-,21-/m1/s1

171764-49-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4R) CIS-(2,4-DIFLUOROPHENYL)-2-(1,2,4-TRIAZOLE-1-YL-METHYL)-1,3-DIOXOLANE-4YL-METHYL-P-TOLYSULFONATE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:171764-49-1 SDS

171764-49-1Downstream Products

171764-49-1Relevant articles and documents

Synthesis and in vitro and in vivo structure-activity relationships of novel antifungal triazoles for dermatology

Meerpoel, Lieven,Backx, Leo J. J.,Van Der Veken, Louis J. E.,Heeres, Jan,Corens, David,De Grout, Alex,Odds, Frank C.,Van Gerven, Frans,Woestenborghs, Filip A. A.,Van Breda, Andre,Oris, Michel,Van Dorsselaer, Pascal,Willemsens, Gustaaf H. M.,Vermuyten, Karen J. P.,Marichal, Patrick J. M. G.,Vanden Bossche, Hugo F.,Ausma, Jannie,Borgers, Marcel

, p. 2184 - 2193 (2007/10/03)

In search for new compounds with potential for clinical use as antifungal agents in dermatology, a series of 12 azole compounds were synthesized stereospecifically and investigated specifically for their activity against dermatophyte fungal infections in

[[4-[4-(4-phenyl-1-piperazinyl)phenoxymethyl]-1,3-dioxolan-2-yl]methyl]-1H-imidazoles and 1H-1,2,4-triazoles having anti-microbial properties

-

, (2008/06/13)

Novel [[4-[4-(4-phenyl-1-piperazinyl)phenoxymethyl]-1,3-dioxolan-2-yl]methyl]-1H-imidazoles and 1H-1,2,4-triazoles, having anti-microbial activity, compositions containing the same, and methods of inhibiting and/or eliminating the development of fungi and

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