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224047-41-0

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  • 1-[2-(4-CHLOROPHENYL)-1-(1-HYDROXY-1-PHENYLETHYL)ETHYL]-1,2,4-TRIAZOLE

    Cas No: 224047-41-0

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224047-41-0 Usage

Description

1-[2-(4-CHLOROPHENYL)-1-(1-HYDROXY-1-PHENYLETHYL)ETHYL]-1,2,4-TRIAZOLE is a chemical compound belonging to the triazole family. It is characterized by its unique molecular structure, which features a 1,2,4-triazole ring fused with a phenyl group and an ethyl group. 1-[2-(4-CHLOROPHENYL)-1-(1-HYDROXY-1-PHENYLETHYL)ETHYL]-1,2,4-TRIAZOLE has potential applications in various fields due to its distinct chemical properties.

Uses

Used in Plant Growth Regulation:
1-[2-(4-CHLOROPHENYL)-1-(1-HYDROXY-1-PHENYLETHYL)ETHYL]-1,2,4-TRIAZOLE is used as a plant growth regulator for the inhibition of brassinosteroid biosynthesis. This application is particularly relevant in the study of plant growth and development, as brassinosteroids play a crucial role in these processes. By inhibiting brassinosteroid biosynthesis, this compound can induce morphological changes in plants, such as dwarfism, altered leaf color, and curling.
Used in Pharmaceutical Industry:
1-[2-(4-CHLOROPHENYL)-1-(1-HYDROXY-1-PHENYLETHYL)ETHYL]-1,2,4-TRIAZOLE may also have potential applications in the pharmaceutical industry, given its unique chemical structure. It could be used as a starting material or intermediate in the synthesis of various drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Research:
1-[2-(4-CHLOROPHENYL)-1-(1-HYDROXY-1-PHENYLETHYL)ETHYL]-1,2,4-TRIAZOLE can be utilized in chemical research to explore its reactivity, stability, and potential interactions with other molecules. Understanding these properties can lead to the development of new compounds with specific applications in various industries, such as agriculture, pharmaceuticals, or materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 224047-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,0,4 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 224047-41:
(8*2)+(7*2)+(6*4)+(5*0)+(4*4)+(3*7)+(2*4)+(1*1)=100
100 % 10 = 0
So 224047-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H18ClN3O/c1-18(23,15-5-3-2-4-6-15)17(22-13-20-12-21-22)11-14-7-9-16(19)10-8-14/h2-10,12-13,17,23H,11H2,1H3

224047-41-0 Well-known Company Product Price

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  • TCI America

  • (B2829)  Brassinazole  >93.0%(HPLC)

  • 224047-41-0

  • 10mg

  • 3,800.00CNY

  • Detail
  • TCI America

  • (B2829)  Brassinazole  >93.0%(HPLC)

  • 224047-41-0

  • 100mg

  • 9,900.00CNY

  • Detail

224047-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorophenyl)-2-phenyl-3-(1,2,4-triazol-1-yl)butan-2-ol

1.2 Other means of identification

Product number -
Other names 1-[2-(4-Chlorophenyl)-1-(1-hydroxy-1-phenylethyl)ethyl]-1,2,4-triazole

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:224047-41-0 SDS

224047-41-0Downstream Products

224047-41-0Relevant articles and documents

Enantioselective palladium-catalyzed diboration of 1,1-disubstituted allenes

Liu, Jiawang,Nie, Ming,Zhou, Qinghai,Gao, Shen,Jiang, Wenhao,Chung, Lung Wa,Tang, Wenjun,Ding, Kuiling

, p. 5161 - 5165 (2017)

A practical and enantioselective palladium-catalyzed diboration of 1,1-disubstituted allenes is developed by employing a P-chiral monophosphorus ligand, BI-DIME. A series of diboronic esters containing a chiral tertiary boronic ester moiety are formed in excellent yields and ee's with the palladium loading as low as 0.2 mol%. DFT calculations revealed a concerted mechanism of oxidative addition of bis(pinacolato)diboron and allene insertion, as well as a critical dispersion effect on the origins of the enantioselectivity. The method is successfully applied to the concise and enantioselective synthesis of brassinazole.

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