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34693-23-7

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  • [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methyl dihydrogenphosphate

    Cas No: 34693-23-7

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34693-23-7 Usage

General Description

The chemical compound "[2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid" is a complex organic molecule containing a phosphonic acid group. It consists of a five-membered ring with three hydroxyl groups and a phosphonooxymethyl group attached to the second carbon atom of the ring. Additionally, it contains a methoxyphosphonic acid group attached to the oxygen atom of the ring. [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid has potential applications in various fields, including pharmaceuticals, agriculture, and materials science, due to its unique structure and properties. Further research and exploration of this compound may reveal its potential uses and benefits.

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.

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