Cas 87598-97-8,benzyl 5,6-anhydro-2,3-O-(1-methylethylidene)-β-D-gulofuranoside

87598-97-8

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Basic information

Product Name: benzyl 5,6-anhydro-2,3-O-(1-methylethylidene)-β-D-gulofuranoside
Synonyms: benzyl 5,6-anhydro-2,3-O-(1-methylethylidene)-β-D-gulofuranoside
CAS NO:87598-97-8
Molecular Formula:
Molecular Weight: 292.332
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: benzyl 5,6-anhydro-2,3-O-(1-methylethylidene)-β-D-gulofuranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 5,6-anhydro-2,3-O-(1-methylethylidene)-β-D-gulofuranoside(87598-97-8)
EPA Substance Registry System: benzyl 5,6-anhydro-2,3-O-(1-methylethylidene)-β-D-gulofuranoside(87598-97-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 87598-97-8(Hazardous Substances Data)

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87598-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87598-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,9 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87598-97:
(7*8)+(6*7)+(5*5)+(4*9)+(3*8)+(2*9)+(1*7)=208
208 % 10 = 8
So 87598-97-8 is a valid CAS Registry Number.

87598-97-8Upstream product

74912-02-0 (R)-1-((3aR,4R,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-ethane-1,2-diol

87598-97-8Downstream Products

87598-98-9 benzyl 6-deoxy-2,3-O-(1-methylethylidene)-β-D-gulofuranoside

87598-97-8Relevant academic research and scientific papers

Total Synthesis of Polyether Antibiotics. Synthesis of the Enantiomer of Lasalocid A (X-537A)

Ireland, Robert E.,Courtney, Lawrence,Fitzsimmons, Brian J.

, p. 5186 - 5198 (1983)

A convergent total synthesis of the enantiomer of lasalocid A (X-537A) and the preliminary results of the biological testing of this compound are reported.

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