58670-14-7 Usage
Chemical compound
A substance formed by a chemical reaction, often used in organic synthesis and carbohydrate chemistry.
Derivative of fructose
A simple sugar found in many fruits and honey, used as a starting material for the synthesis of complex carbohydrates.
Benzoyl groups
Four benzoyl groups are attached to the fructose molecule, providing stability and allowing for further manipulations in chemical reactions.
Preparation of complex carbohydrates
The compound is commonly used in the preparation of complex carbohydrates, which are essential components of many biological systems.
Building block
It serves as a building block in the synthesis of various natural products, including bioactive compounds.
Carbohydrate chemistry
The compound has been widely studied and utilized in the field of carbohydrate chemistry for its ability to serve as a valuable intermediate in the synthesis of many bioactive compounds.
Structure
The structure of 1,3,4,6-Tetra-O-benzoyl-a-D-fructofuranose consists of a fructose molecule with four benzoyl groups attached at the 1, 3, 4, and 6 positions.
Stability
The presence of benzoyl groups in the compound provides stability, making it suitable for use in various chemical reactions and synthesis processes.
Further manipulations
The compound's structure allows for further manipulations in chemical reactions, making it a versatile building block for the synthesis of complex molecules.
Bioactive compounds
The compound is used as an intermediate in the synthesis of many bioactive compounds, which have potential applications in the pharmaceutical and biotechnology industries.
Check Digit Verification of cas no
The CAS Registry Mumber 58670-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58670-14:
(7*5)+(6*8)+(5*6)+(4*7)+(3*0)+(2*1)+(1*4)=147
147 % 10 = 7
So 58670-14-7 is a valid CAS Registry Number.
58670-14-7Relevant articles and documents
Enzymatic procedures in the preparation of regioprotected D-fructose derivatives
D'Antona, Nicola,El-Idrissi, Mostafa,Ittobane, Najim,Nicolosi, Giovanni
, p. 319 - 323 (2005)
A combination of different lipases from Pseudomonas cepacia, Candida antarctica B, Candida rugosa and Mucor miehei, aided the regioesterification of the free fructose allowing the synthesis of 1,6-di-O-acetyl-d-fructofuranose, 1,4,6-tri-O-acetyl-d-fructofuranose, 1,6-di-O-acetyl-4-O-benzoyl-d- fructofuranose and 1,6-di-O-benzoyl-d-fructofuranose. Using C. antarctica B and C. rugosa lipases the alcoholysis of fructose peracetate (α, β-form) has furnished 1,2,3,4-tetra-O-acetyl-α-d-fructofuranose and 2,3,4,6-tetra-O-acetyl-β-d-fructofuranose. 1,4,6-Tri-O-acetyl-d- fructofuranose was successfully employed to produce a rare ketohexose, namely d-psicose.
SYNTHESIS OF L-IDARO-1,4-LACTONE, AN INHIBITOR OF α-L-IDOSID-URONASE
Herd, J. Kenneth,Mayberry, William R.,Snell, Robert L.
, p. 33 - 40 (2007/10/02)
L-Idaro-1,4-lactone was synthesized by two different, published methods: (1) epimerization of monopotassium D-glucarate by refluxing in aqueous barium hydroxide, and (2) oxidation of L-iditol by heating in dilute nitric acid.The lactone, formed by heat dehydration from aqueous solution at low pH, was purified by paper chromatography, and quantitated by gas-liquid chromatography using inositol as the internal standard.The monolactone inhibited human, seminal-fluid α-L-idosiduronase activity, with either phenyl or 4-methylumbelliferyl α-L-idosiduronic acid as the substrate, to the same degree as D-glucaro-1,4-lactone inhibits α-D-glucosiduranose.
