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117211-21-9

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117211-21-9 Usage

Description

N-[1-(3-Chlorphenyl)benzyl]urea is a urea derivative chemical compound, characterized by its white crystalline solid appearance and a molecular formula of C15H13ClN2O. It has been the subject of research for its potential as an antidiabetic agent, with studies suggesting its capacity to reduce blood glucose levels. Furthermore, it has demonstrated insecticidal properties, positioning it as a candidate for use in agriculture against pests. N-[1-(3-Chlorphenyl)benzyl]urea's multifaceted biological activities have garnered interest in both pharmaceutical and agricultural sectors.

Uses

Used in Pharmaceutical Industry:
N-[1-(3-Chlorphenyl)benzyl]urea is used as an antidiabetic agent for its potential to lower blood glucose levels, offering a new avenue for the treatment of diabetes.
Used in Agricultural Industry:
N-[1-(3-Chlorphenyl)benzyl]urea is used as an insecticide for its bioactivity against agricultural pests, providing a potential solution for pest control in farming.

Check Digit Verification of cas no

The CAS Registry Mumber 117211-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,2,1 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 117211-21:
(8*1)+(7*1)+(6*7)+(5*2)+(4*1)+(3*1)+(2*2)+(1*1)=79
79 % 10 = 9
So 117211-21-9 is a valid CAS Registry Number.

117211-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3-chlorophenyl)-phenylmethyl]urea

1.2 Other means of identification

Product number -
Other names m-chlorobenzhydrylurea

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:117211-21-9 SDS

117211-21-9Relevant articles and documents

The determination of enantiomer composition of 1‐((3‐chlorophenyl)‐(phenyl)methyl) amine and 1‐((3‐chlorophenyl)(phenyl)‐methyl) urea (galodif) by nmr spectroscopy, chiral hplc, and polarimetry

Kuksenok, Vera Yu.,Shtrykova, Victoria V.,Filimonov, Victor D.,Druganov, Alexandr G.,Bondarev, Alexandr A.,Stankevich, Ksenia S.

, p. 1135 - 1143 (2018)

For the first time, a method for enantiomer resolution of the anticonvulsant Galodif (1‐((3‐chlorophenyl)(phenyl)methyl) urea) by chiral HPLC was developed, whereas the enantiomeric composition of 1‐((3‐chlorophenyl)(phenyl) methyl) amine—precursor in Galodif synthesis—cannot be resolved by this method. However, starting 1‐((3‐chlorophenyl)(phenyl)methyl) amine quantitatively forms diastereomeric N‐((3‐chlorophenyl)(phenyl)methyl)‐1‐ camphorsulfonamides in reaction with chiral (1R)‐(+)‐ or (1S)‐(?)‐camphor‐10‐ sulfonyl chlorides. The diastereomeric ratio of obtained camphorsulfonamides can be easily determined by NMR1H and13C spectroscopy. The DFT calculations of specific rotation of Galodif enantiomers showed good agreement with experimental data. The absolute configuration of enantiomers was proposed for the first time.

QUANTITATUVE RELATIONSHIP BETWEEN ANTICONVULSANT ACTIVITY IN N-BENZHYDRYLAMIDES AND N-BENZHYDRYLURAES, THEIR STRUCTURES, AND (13)C NMR SPECTRA

Filimonov, V. D.,Bakibaev, A. A.,Pustovoitov, A. V.,Tignibidina, L. G.,Pechenkin, A. G.,et al.

, p. 358 - 363 (2007/10/02)

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