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19071-54-6

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19071-54-6 Usage

General Description

1-(alpha-(Hydroxymethyl)phenethyl)-3-phenylurea, also known as fenhexamid, is a chemical compound used as a fungicide in agricultural applications. It belongs to the group of phenylurea fungicides and is effective against a wide range of fungal diseases, particularly those affecting fruits and vegetables. Fenhexamid works by inhibiting the enzyme responsible for the synthesis of fungal cell walls, ultimately leading to the death of the fungus. It has low toxicity to mammals and is considered to be environmentally friendly due to its low impact on non-target organisms. However, like all chemical compounds, it is important to handle fenhexamid with caution and follow appropriate safety measures when using it.

Check Digit Verification of cas no

The CAS Registry Mumber 19071-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,7 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19071-54:
(7*1)+(6*9)+(5*0)+(4*7)+(3*1)+(2*5)+(1*4)=106
106 % 10 = 6
So 19071-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H18N2O2/c19-12-15(11-13-7-3-1-4-8-13)18-16(20)17-14-9-5-2-6-10-14/h1-10,15,19H,11-12H2,(H2,17,18,20)

19071-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-hydroxy-3-phenylpropan-2-yl)-3-phenylurea

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:19071-54-6 SDS

19071-54-6Downstream Products

19071-54-6Relevant articles and documents

Microwave-assisted synthesis of bidentate chiral unsymmetrical urea derivatives of p-tert-butylcalix[4]arene and their anion recognition properties

Wang, Xiaohong,Zhao, Zhigang,Chen, Bailing,Li, Xiaoxiao,Liu, Min

, p. 303 - 306 (2015)

Four new derivatives of p-t-butylcalix[4]arene containing two (1,3-distal) chiral unsymmetrical urea moieties at the lower rim were synthesised in four steps. Their anion recognition properties toward MeCO2-, H2PO4-, NOsu

Solvent-free synthesis of novel chiral unsymmetrical urea molecular tweezers under microwave irradiation

Zhao, Zhigang,Xia, Zhenyang,Li, Xiaorui,Shi, Peiyu

scheme or table, p. 47 - 50 (2011/05/04)

Seven novel chiral unsymmetrical urea molecular tweezers based on 1, 3-phenoxyacetic acid have been designed and synthesised using solid K 2CO3 as supporter in the solvent-free conditions under microwave irradiation. This method is simple, fast, efficient and eco-friendly. The structures of target compounds were characterised by IR, 1H NMR, MS spectra and elemental analyses and their molecular recognition properties were investigated by UV-Vis spectral titration. The preliminary results indicated that these molecular tweezers possess good selectivity for D/L amino acid methyl esters and some anions.

Investigation of the Mitsunobu reaction of N-(2-hydroxyethyl)-N'- phenyl-ureas

Kim, Taek Hyeon,Lee, Gue-Jae,Cha, Mi-Hyun

, p. 2753 - 2758 (2007/10/03)

The Mitsunobu reaction of N-(2-hydroxyethyl)-ureas 1 using PPh3 and EtO2CN=NCO2Et led to the mixture of N- and O-alkylation products or a single isomer depending on the substrates.

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