Welcome to LookChem.com Sign In|Join Free
  • or
1-[(2E)-3-methyl-1,3-thiazolidin-2-ylidene]-3-[(2Z)-3-methyl-1,3-thiazolidin-2-ylidene]urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73696-64-7

Post Buying Request

73696-64-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

73696-64-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

Urea derivatives are compounds that have a urea group (NH2-CO-NH2) as part of their structure.

Explanation

Thiazolidine is a five-membered heterocyclic compound containing sulfur and nitrogen atoms. The compound has two such rings.

Explanation

Thiazolidinylidene is a type of carbene, which is a molecule containing a neutral carbon atom with six electrons. The compound has two such groups attached to the urea molecule.

Explanation

The compound has two thiazolidinylidene groups with different stereochemistry, one in the (2E) configuration and the other in the (2Z) configuration.

Explanation

Due to its unique structure and properties, the compound may have potential uses in various fields, including the development of new drugs and materials.

Explanation

The compound's structure is characterized by a central urea molecule with two thiazolidine rings attached, forming a carbon-nitrogen-carbon-nitrogen backbone.

Explanation

The presence of sulfur and nitrogen atoms in the thiazolidine rings classifies the compound as a heterocyclic compound.

Explanation

The thiazolidinylidene groups in the compound are carbenes, which are molecules containing a neutral carbon atom with six electrons.

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule, which in this case is approximately 256.39 g/mol.

Urea derivative

Contains a urea molecule

Thiazolidine rings

Contains two thiazolidine rings

Thiazolidinylidene groups

Contains two thiazolidinylidene groups

Stereochemistry

(2E) and (2Z) configurations

Potential applications

Medicinal chemistry, drug development, materials science, and other chemical industries

Chemical structure

Contains a carbon-nitrogen-carbon-nitrogen backbone

Heterocyclic compound

Contains both sulfur and nitrogen atoms

Carbene-containing compound

Contains neutral carbon atoms with six electrons

Molecular weight

Approximately 256.39 g/mol

Check Digit Verification of cas no

The CAS Registry Mumber 73696-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73696-64:
(7*7)+(6*3)+(5*6)+(4*9)+(3*6)+(2*6)+(1*4)=167
167 % 10 = 7
So 73696-64-7 is a valid CAS Registry Number.

73696-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z,3E)-1,3-bis(3-methyl-1,3-thiazolidin-2-ylidene)urea

1.2 Other means of identification

Product number -
Other names Urea,1,3-bis(3-methyl-2-thiazolidinylidene)

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:73696-64-7 SDS

73696-64-7Downstream Products

73696-64-7Relevant academic research and scientific papers

Inhibitors of indoleethylamine N-methyltransferase. Derivatives of 3-methyl-2-thiazolidinimine. In vitro, in vivo, and metabolic studies

Rokach,Girard,Hamel,Reader,Rooney,Mandel,Cragoe Jr.,Zacchei

, p. 773 - 780 (2007/10/02)

A variety of substituent groups has been attached to the exocyclic imine function of 2-imino-3-methylthiazolidine in a search for metabolic precursors of this potent inhibitor of the enzyme indoleethylamine N-methyltransferase (INMT) which would exhibit s

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 73696-64-7