1,2-O-Isopropylidene-α-D-Glucurono-6,3-Lactone

Basic information

  • Product Name:1,2-O-Isopropylidene-α-D-Glucurono-6,3-Lactone
  • CasNo.:20513-98-8
  • MF:C9H12O6
  • MW:216.191

Physical and Chemical Properties

  • Boiling Point:119-121 °C
  • Packing:
  • Throughput:
Inquiry

Product Details

CasNo: 20513-98-8

MF: C9H12O6

Factory Export Top Purity 1,2-O-Isopropylidene-α-D-Glucurono-6,3-Lactone 20513-98-8 In Stock

Synonyms: 1,2-O-Isopropylidene-α-D-glucofuranurono-6,3-lactone;D-Glucorono-6,3-lactone acetonide

Molecular Formula:  C9H12O6

Molecular Weight: 216.19 

CAS Number20513-98-8

Molecular Structure:

Item

Specification

Appearance

White to off-white crystalline powder

Assay (GC),%

≥98.0

Melting Point, ℃

119.0~123.0

Loss on drying,%

≤0.5

Residue on ignition,%

≤0.10

D-Glucurono-6,3-lactone acetonide(Cas 20513-98-8) Usage

Glycoside pharmaceutical intermediates

20513-98-8 Relevant articles

Attempted synthesis of the imidazylate of an α-hydroxylactone results in unexpected chlorination: Synthesis and X-ray crystal structure of 5-Chloro-5-deoxy-1,2- O -isopropylidene-β- l -idurono-6,3-lactone

Mohamed, Shifaza,Bernhardt, Paul V.,Ferro, Vito

, p. 197 - 205 (2014)

Attempted synthesis of the imidazylate d...

Preparation of derivatives of L-idose and L-iduronic acid from 1,2-O-isopropylidene-alpha-D-glucofuranose by way of acetylenic intermediates.

Horton,Tsai

, p. 89 - 108,92,95,103 (1977)

The products (1) from the periodate oxid...

A novel synthesis of L ascorbic acid

Kitahara,Ogawa,Naganuma,Matsui

, p. 2189 - 2190 (1974)

-

Synthesis of 1,3,4,6-Tetra-O-acetyl-l-gulose

Che, Rui,Liu, Xingui,Lu, Wei

, p. 237 - 241 (2017)

A novel, practical and concise synthesis...

Efficient Divergent Synthesis of 2′- O,4′- C-Ethylene-Bridged Nucleic Acid (ENA) Phosphoramidites

Abe, Yuzo,Michida, Makoto,Ukai, Kazutoshi

, (2022/04/07)

2′-O,4′-C-Ethylene-bridged nucleic acid ...

Method for preparing eribulin dehydroxylation intermediate by one-pot method

-

Paragraph 0025-0026, (2021/09/08)

The invention relates to the technical f...

INTERMEDIATES FOR THE PREPARATION OF ERIBULIN THEREOF

-

Page/Page column 8, (2019/06/11)

The present invention relates to novel i...

20513-98-8 Process route

D-glucurono-6,3-lactone

D-glucurono-6,3-lactone

acetone
67-64-1

acetone

D-glucurono-3,6-lactone acetonide
3067-56-9,20513-98-8,25159-39-1,26623-22-3,29514-28-1,85080-95-1

D-glucurono-3,6-lactone acetonide

Conditions
Conditions Yield
D-glucurono-6,3-lactone; acetone; In acetonitrile; at 50 ℃; for 0.5h; Molecular sieve;
With sulfuric acid; for 8h; Reflux;
90%
D-glucurono-6,3-lactone
63-29-6,487-44-5,575-64-4,14362-29-9,18281-92-0,26623-21-2

D-glucurono-6,3-lactone

acetone
67-64-1

acetone

D-glucurono-3,6-lactone acetonide
3067-56-9,20513-98-8,25159-39-1,26623-22-3,29514-28-1,85080-95-1

D-glucurono-3,6-lactone acetonide

Conditions
Conditions Yield
With sulfuric acid;
93%
With sulfuric acid; for 5h;
90%
With sulfuric acid; at 20 ℃; for 4h; Inert atmosphere;
90%
With toluene-4-sulfonic acid; copper(II) sulfate;
87%
With sulfuric acid; at 20 ℃; for 38h;
84%
With sulfuric acid;
82%
With sulfuric acid; at 20 ℃; for 5h;
79%
With acid;
78%
With sulfuric acid;
 
sulfuric acid; In acetonitrile; at 25 ℃; for 18h; Heating / reflux;
 
With sulfuric acid; at 20 ℃;
 
With sulfuric acid; In acetonitrile; at 65 ℃;
 
With sulfuric acid;
100 mg
With sulfuric acid; at 10 - 35 ℃; Inert atmosphere;
 

20513-98-8 Upstream products

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20513-98-8 Downstream products

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    1,2-O-isopropylidene-5-O-toluene-p-sulphonyl-α-D-glucofuranurono-6,3-lactone

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    D-glucose

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    1,2-O-isopropylidene-α-D-glucofuranose

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    methyl 3,5-O-benzylidene-1,2-O-isopropylidene-α-D-glucofuranuronate