2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONE

Product Name
2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONE
CAS No.
51607-16-0
Chemical Name
2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONE
Synonyms
2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTOL;(-)-2,3-O-ISOPROPYLIDENE-D-ERYTHRONO-LACTONE;1,3-Dioxolane-4-carboxaldehyde, 5-(hydroxymethyl)-2,2-dimethyl-, (4R,5R)-
CBNumber
CB3412226
Molecular Formula
C7H12O4
Formula Weight
160.17
MOL File
51607-16-0.mol
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2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONE Property

Melting point:
67-69 °C(lit.)
Boiling point:
249.1±25.0 °C(Predicted)
Density 
1.192±0.06 g/cm3(Predicted)
pka
14.20±0.10(Predicted)
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM0007780
Product name
2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTOL
Purity
95.00%
Packaging
1G
Price
$696.24
Updated
2021/12/16

2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONE Preparation Products And Raw materials

Raw materials

Preparation Products

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2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONE Suppliers

Canada 1 China 2 Germany 2 Switzerland 1 United Kingdom 2 United States 3 Global 11
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
Advanced Technology & Industrial Co., Ltd.
Tel
--
Fax
--
Email
sales@advtechind.com
Country
China
ProdList
6523
Advantage
75

51607-16-0, 2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONERelated Search:

Sodium erythorbate Ribose Stevioside Erythromycin thiocyanate D-ERYTHRONOLACTONE 2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTONE 1,3-Butadiene diepoxide Erythritol erythrose-4-phosphate 1,4-Dithioerythritol tetraacetate Erythorbic Acid Dithioerythritol eritrityl tetranitrate

  • 2,3-O-ISOPROPYLIDENE-D-ERYTHRONOLACTOL
  • (-)-2,3-O-ISOPROPYLIDENE-D-ERYTHRONO-LACTONE
  • 1,3-Dioxolane-4-carboxaldehyde, 5-(hydroxymethyl)-2,2-dimethyl-, (4R,5R)-
  • 51607-16-0
  • Carbohydrate Synthesis
  • O-Substituted Sugars
  • Sugars
  • Erythrose
  • Sugar Acids
  • Monosaccharides
  • Specialty Synthesis