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1H-1,2,4-Triazole-1-propanol, b-(2,4-dichlorophenyl)-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131216-56-3

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131216-56-3 Usage

Chemical class

triazole fungicides

Chirality

chiral molecule with (S)-enantiomer being the biologically active form

Use

control fungal diseases in a wide range of crops, including fruits, vegetables, and ornamentals

Mechanism of action

inhibits the growth of fungi and prevents the formation of fungal cell membranes

Potency

(S)-enantiomer is more potent and important in the development of new fungicides with increased efficacy

Role in agriculture

protects crops from fungal infections and improves yields.

Check Digit Verification of cas no

The CAS Registry Mumber 131216-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,1 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 131216-56:
(8*1)+(7*3)+(6*1)+(5*2)+(4*1)+(3*6)+(2*5)+(1*6)=83
83 % 10 = 3
So 131216-56-3 is a valid CAS Registry Number.

131216-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-(2,4-Dichloro-phenyl)-3-[1,2,4]triazol-1-yl-propan-1-ol

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

More Details:131216-56-3 SDS

131216-56-3Upstream product

131216-56-3Relevant academic research and scientific papers

Enzymatic preparation of optically active fungicide intermediates in aqueous and in organic media

Bianchi, Daniele,Cesti, Pietro,Golini, Paolo,Spezia, Sandro,Garavaglia, Carlo,Mirenna, Luigi

, p. 176 - 180 (2007/10/02)

Pure stereoisomers of two new triazole and morpholine fungicides have been prepared starting from enzymatically synthesized chiral alcohol intermediates.Two resolution strategies compared are: lipase-catalyzed hydrolysis of corresponding acetates in water and lipase-catalyzed transesterification of alcohols in organic solvents.The antifungal activity of optically pure enantiomers of the synthesized fungicides investigated in vitro and in vivo against a variety of fungi, show an activity ratio (R-form/S-form) up to 400.

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