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1467-21-6

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1467-21-6 Usage

General Description

1-benzyl-3-phenylurea is a chemical compound with the molecular formula C15H14N2O. It is a urea derivative that is commonly used as a plant growth regulator to promote lateral branching and flowering in various crops. 1-benzyl-3-phenylurea has been found to significantly improve fruit set and yield in different plants, including grapes, kiwifruit, and tomatoes. Additionally, it has been shown to enhance the quality and shelf life of fruits by increasing their sugar content and reducing physiological disorders. This chemical compound is also used in the pharmaceutical industry as a potential therapeutic agent and in organic chemistry as a reagent for various synthetic transformations. Despite its beneficial effects, caution should be exercised when handling 1-benzyl-3-phenylurea, as it may pose health and environmental hazards if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1467-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1467-21:
(6*1)+(5*4)+(4*6)+(3*7)+(2*2)+(1*1)=76
76 % 10 = 6
So 1467-21-6 is a valid CAS Registry Number.

1467-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-phenylurea

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-benzylurea

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:1467-21-6 SDS

1467-21-6Relevant articles and documents

Curtius-like Rearrangement of an Iron-Nitrenoid Complex and Application in Biomimetic Synthesis of Bisindolylmethanes

Li, Dashan,Wu, Ting,Liang, Kangjiang,Xia, Chengfeng

, p. 2228 - 2231 (2016)

A Curtius-like rearrangement of hydroxamates to isocyanates was discovered. This reaction was initiated from an iron(II)-nitrenoid complex, which was generated by the iron(II)-catalyzed cleavage of N-O bonds of functionalized hydroxamates. To demonstrate the efficiency of this new Curtius-like rearrangement in synthetic chemistry, a biomimetic strategy for the one-pot preparation of bisindolylmethanes was developed.

Broad Scope and High-Yield Access to Unsymmetrical Acyclic [11C]Ureas for Biomedical Imaging from [11C]Carbonyl Difluoride

Jakobsson, Jimmy E.,Jana, Susovan,Lu, Shuiyu,Pike, Victor W.,Telu, Sanjay

supporting information, p. 10369 - 10376 (2021/06/07)

Effective methods are needed for labelling acyclic ureas with carbon-11 (t1/2=20.4 min) as potential radiotracers for biomedical imaging with positron emission tomography (PET). Herein, we describe the rapid and high-yield syntheses of unsymmet

Stabilization of the hindered urea bond through de-tert-butylation

Yang, Yingfeng,Ying, Hanze,Jia, Yunchao,Chen, Yingying,Cheng, Jianjun

supporting information, p. 3812 - 3815 (2021/04/21)

We report the discovery of an acid-assisted de-tert-butylation reaction that can instantly “turn off” the dynamicity of hindered urea bonds (HUBs) and thus broaden their applications. The reaction is demonstrated to be widely applicable to different hindered urea substrates, leading to improved chemical stabilities and mechanical properties of HUB-containing materials.

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