Welcome to LookChem.com Sign In|Join Free

CAS

  • or

36033-33-7

Post Buying Request

36033-33-7 Suppliers

Recommended suppliersmore

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

36033-33-7 Usage

Description

5,5-DIPROPYL-IMIDAZOLIDINE-2,4-DIONE, a chemical compound with the molecular formula C9H16N2O2, is a derivative of imidazolidine-2,4-dione featuring two propyl groups attached to the nitrogen atom. Classified as a cyclic urea, this compound plays a significant role in the synthesis of pharmaceuticals and agrochemicals, and holds potential for new material development and as a reagent in organic chemistry reactions. Due to its potential health hazards and environmental risks, it is crucial to handle and use 5,5-DIPROPYL-IMIDAZOLIDINE-2,4-DIONE according to proper safety guidelines.

Uses

Used in Pharmaceutical Industry:
5,5-DIPROPYL-IMIDAZOLIDINE-2,4-DIONE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with unique therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 5,5-DIPROPYL-IMIDAZOLIDINE-2,4-DIONE is utilized as a precursor in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Material Science:
5,5-DIPROPYL-IMIDAZOLIDINE-2,4-DIONE is employed in the development of new materials, leveraging its chemical properties to engineer innovative substances with specific applications in various industries.
Used as a Reagent in Organic Chemistry:
5,5-DIPROPYL-IMIDAZOLIDINE-2,4-DIONE serves as a reagent in organic chemistry reactions, facilitating various synthetic processes and transformations that are essential for the advancement of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 36033-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36033-33:
(7*3)+(6*6)+(5*0)+(4*3)+(3*3)+(2*3)+(1*3)=87
87 % 10 = 7
So 36033-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H16N2O2/c1-3-5-9(6-4-2)7(12)10-8(13)11-9/h3-6H2,1-2H3,(H2,10,11,12,13)

36033-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dipropylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5,5-dipropyl-imidazolidine-2,4-dione

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:36033-33-7 SDS

36033-33-7Downstream Products

36033-33-7Relevant articles and documents

Supramolecular architectures in 5,5′-substituted hydantoins: Crystal structures and Hirshfeld surface analyses

Chattopadhyay, Basab,Mukherjee, Alok K.,Narendra,Hemantha,Sureshbabu, Vommina V.,Helliwell, Madeliene,Mukherjee, Monika

, p. 4476 - 4484 (2010)

A series of three 5,5′-substituted hydantoin derivatives (1-3) were synthesized, and their crystal structures were solved using single-crystal synchrotron/powder-crystal X-ray diffraction data with a detailed analysis of Hirshfeld surfaces and fingerprint plots facilitating a comparison of intermolecular interactions in building different supramolecular architectures. A comparison of supramolecular assembly in the compounds with that in similar 5,5′-substituted hydantoins in the Cambridge Structural Database (CSD) has been presented. The crystal packing in compounds 1-3 containing complementary hydrogen bonding groups, i.e. the amino NH donors and carbonyl O acceptors, exhibits three types of supramolecular synthons. In the dipropyl substituted hydantoin (1), intermolecular N-H...O hydrogen bonds with only one carbonyl O atom acting as a double acceptor generate a one-dimensional C 11(4)C11(4)[R2 2(8)] network propagating along the [100] direction, while in 3, a 5-spiro fused hydantoin, the cyclic R22(8) motifs self-organize through pairs of N-H...O hydrogen bonds to form a C 22(9)[R22(8)][R2 2(8)] framework running along the [1-10] direction. The molecular assembly in 2, with a dibutyl substitution at the hydantoin C-5 position, produces R44(17) synthons, which are edge-fused to form two-dimensional molecular sheets in the (100) plane. The formation of a supramolecular architecture built with an R44(17) synthon is unprecedented among the substituted hydantoin structures in the CSD.

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

What can I do for you?
Get Best Price

Get Best Price for 36033-33-7