Welcome to LookChem.com Sign In|Join Free

CAS

  • or

34693-23-7

Post Buying Request

34693-23-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methyl dihydrogenphosphate

    Cas No: 34693-23-7

  • No Data

  • No Data

  • No Data

  • BOC Sciences
  • Contact Supplier

34693-23-7 Usage

Description

[2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid is a complex organic molecule characterized by a five-membered oxolan ring with three hydroxyl groups and a phosphonooxymethyl group attached to the second carbon atom. It also features a methoxyphosphonic acid group connected to the oxygen atom of the ring. This unique structure endows the compound with potential applications across various industries, including pharmaceuticals, agriculture, and materials science.

Uses

Used in Pharmaceutical Applications:
[2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid is used as a potential therapeutic agent for various medical conditions due to its unique structure and properties. Its phosphonic acid group may offer advantages in targeting specific biological processes, making it a candidate for drug development and treatment of certain diseases.
Used in Agricultural Applications:
In the agricultural industry, [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid may be utilized as a component in the development of novel pesticides or fertilizers. Its complex structure could provide new ways to enhance crop yield, protect plants from pests, or improve nutrient uptake.
Used in Materials Science:
[2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid's unique chemical structure may also find applications in materials science. It could be used in the development of new materials with specific properties, such as improved strength, durability, or chemical resistance, depending on the needs of various industries.
Further research and exploration of [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid are necessary to fully understand its potential uses and benefits across these industries. As our knowledge of this compound grows, so too will the range of applications it can be utilized in.

Check Digit Verification of cas no

The CAS Registry Mumber 34693-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,9 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34693-23:
(7*3)+(6*4)+(5*6)+(4*9)+(3*3)+(2*2)+(1*3)=127
127 % 10 = 7
So 34693-23-7 is a valid CAS Registry Number.

34693-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methyl dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names Fructose 1,6-diphosphate

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:34693-23-7 SDS

34693-23-7Downstream Products

34693-23-7Relevant articles and documents

Anomerization of Furanose Sugars and Sugar Phosphates

Pierce, John,Serianni, Anthony S.,Barker, Robert

, p. 2448 - 2456 (2007/10/02)

Thermodynamic and kinetic parameters for the ring-opening and -closing reactions of several aldo- and ketofuanoses and their phosphate esters have been determined by NMR line-width and saturation-transfer methods.Cyclic forms interconvert via a single, acyclic carbonyl form under either acid or base catalysis.Ring-opening rates do not correlate with thermodynamic stability of the rings.For aldofuranose phosphates, α anomers open faster than β anomers; for ketofuranose phosphates the converse is observed.Intramolecular catalysis of anomerization by the phosphate group of sugar phosphates is documented.Biological and mechanistic implications of the observed kinetics are discussed.

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 34693-23-7