Welcome to LookChem.com Sign In|Join Free

CAS

  • or

508-37-2

Post Buying Request

508-37-2 Suppliers

Recommended suppliersmore

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

508-37-2 Usage

Description

Propanedioic acid,2,2-bis[(aminocarbonyl)amino]-, also known as Uroxanic Acid, is an organic compound that serves as an intermediate in the synthesis of various compounds. It is characterized by its unique chemical structure, which includes a propanediol backbone with two aminocarbonyl amino groups attached. This structure grants Uroxanic Acid potential applications in different industries due to its reactivity and ability to form complexes with other molecules.

Uses

Used in Pharmaceutical Industry:
Propanedioic acid,2,2-bis[(aminocarbonyl)amino]is used as an intermediate in the synthesis of Allantoic Acid (A541500) for its role in nucleic acid metabolism. Allantoic Acid is a metabolic intermediate that plays a crucial role in the synthesis and breakdown of nucleic acids, which are essential for cellular function and replication. By facilitating the production of Allantoic Acid, Uroxanic Acid contributes to the development of pharmaceuticals targeting nucleic acid-related conditions and diseases.
Used in Chemical Synthesis:
In the chemical industry, Propanedioic acid,2,2-bis[(aminocarbonyl)amino]is used as a versatile building block for the synthesis of various complex molecules. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the creation of new compounds with potential applications in various fields, such as materials science, pharmaceuticals, and agrochemicals.
Used in Research and Development:
Due to its reactivity and ability to form complexes, Propanedioic acid,2,2-bis[(aminocarbonyl)amino]is also utilized in research and development for the exploration of new chemical reactions and the discovery of novel compounds. Its involvement in the synthesis of Allantoic Acid and other potential applications makes it an interesting subject for scientific investigation, which could lead to the development of new technologies and products in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 508-37-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 508-37:
(5*5)+(4*0)+(3*8)+(2*3)+(1*7)=62
62 % 10 = 2
So 508-37-2 is a valid CAS Registry Number.

508-37-2SDS

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 diureido-malonic acid

1.2 Other means of identification

Product number -
Other names Diureido-malonsaeure

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:508-37-2 SDS

508-37-2Upstream product

508-37-2Downstream Products

508-37-2Relevant articles and documents

THE MECHANISM FOR THE CONVERSION OF URIC ACID INTO UROXANATE AND ALLANTOIN A NEW BASE-INDUCED 1,2-CARBOXYLATE SHIFT

Poje, M.,Sokolic-Maravic, Lea

, p. 6723 - 6728 (1988)

Alkaline permanganate oxidation of uric acid (1), particularly the late stages of the transformation into uroxanate (7) and allantoin (3), was studied by means of isotope-position labelling.A clear-cut degradation procedure developed for distinguishing among carbonyl and α-aminal carbon atoms in these products demonstrated conclusively that the carboxylic carbon of 7 and the 4-carbonyl carbon of 3 have their origin in C(5) of uric acid (1).None of the mechanisms that have been proposed for this reaction would have predicted this result.Isotope-labelling evidence, in combination with other data, revealed the sequence of events and identities of species involved in oxidative transformation of 1; the carbon-skeleton rearrangement of the first transient intermediate 4 must occur by a 1,2-carboxylate shift to give allanatoin-5-carboxylate (6) which either decarboxylates to allantoin (3) or else undergoes hydrolytic ring opening to uroxanate (7).

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 508-37-2