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1,3-bis[(2-methoxyphenyl)methylideneamino]urea is a complex organic compound with the molecular formula C16H18N4O4. It is characterized by two methoxyphenyl groups connected to a central urea unit through methyleneimino bridges. This chemical structure is of interest in various fields, including pharmaceuticals and materials science, due to its potential applications in the development of new drugs and as a building block for advanced materials. The compound's specific properties, such as its reactivity and stability, make it a subject of research for its possible use in the synthesis of more complex molecules.

6341-77-1

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6341-77-1 Usage

Type of compound

Organic compound

Structure

Urea derivative with two 2-methoxyphenylmethylideneamino groups attached to the nitrogen atoms of the urea molecule

Applications

a. Organic synthesis
b. Chemical research
c. Building block for the preparation of various pharmaceuticals and biologically active compounds
d. Development of new materials
e. Reagent in chemical reactions

Importance

Significant chemical in the field of organic chemistry and pharmaceutical research due to its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6341-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6341-77:
(6*6)+(5*3)+(4*4)+(3*1)+(2*7)+(1*7)=91
91 % 10 = 1
So 6341-77-1 is a valid CAS Registry Number.

6341-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(Z)-(2-methoxyphenyl)methylideneamino]-3-[(E)-(2-methoxyphenyl)methylideneamino]urea

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:6341-77-1 SDS

6341-77-1Downstream Products

6341-77-1Relevant academic research and scientific papers

Olive-Shaped Organic Cages: Synthesis and Remarkable Promotion of Hydrazone Condensation through Encapsulation in Water

Xu, Yan-Yan,Liu, Hong-Kun,Wang, Ze-Kun,Song, Bo,Zhang, Dan-Wei,Wang, Hui,Li, Zhiming,Li, Xiaopeng,Li, Zhan-Ting

, p. 3943 - 3951 (2021/03/09)

Two organic cages have been prepared in situ in water through the 2 + 3 hydrazone coupling of two pyridinium-derived trialdehydes and oxalohydrazide. The highly water-soluble cages encapsulate and solubilize linear neutral molecules. Such encapsulation ha

Green synthetic method for 1,5-disubstituted carbohydrazones

Li, Zheng,Zhu, Wei,Yu, Jinlan,Ma, Xuelin,Lu, Zhong,Xiao, Shuxiu

, p. 2613 - 2619 (2007/10/03)

A green synthetic method for 1,5-disubstituted carbohydrazones is described. The reaction of dimethyl carbonate with hydrazine hydrate first gave carbohydrazide, which further reacted with various aromatic aldehydes or aliphatic ketones under solvent-free conditions to efficiently afford 1,5-disubstituted carbohydrazone. This protocol has the advantages of using nontoxic dimethyl carbonate as starting material, no use of organic solvents, short reaction time, high yield, and simple workup procedure. Copyright Taylor & Francis Group, LLC.

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