Cas 615265-09-3,2H,6H,8H-Difuro[3,2-b:3,4-c]furan-6-one, tetrahydro-3,5-dihydroxy-5-methyl-, (3R,3aS,5R,5aS,8aR)- (9CI)

615265-09-3

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Basic information

Product Name: 2H,6H,8H-Difuro[3,2-b:3,4-c]furan-6-one, tetrahydro-3,5-dihydroxy-5-methyl-, (3R,3aS,5R,5aS,8aR)- (9CI)
Synonyms: 2H,6H,8H-Difuro[3,2-b:3,4-c]furan-6-one, tetrahydro-3,5-dihydroxy-5-methyl-, (3R,3aS,5R,5aS,8aR)- (9CI)
CAS NO:615265-09-3
Molecular Formula: C9H12O6
Molecular Weight: 216.18798
EINECS: N/A
Product Categories: ALCOHOL
Mol File: 615265-09-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2H,6H,8H-Difuro[3,2-b:3,4-c]furan-6-one, tetrahydro-3,5-dihydroxy-5-methyl-, (3R,3aS,5R,5aS,8aR)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 2H,6H,8H-Difuro[3,2-b:3,4-c]furan-6-one, tetrahydro-3,5-dihydroxy-5-methyl-, (3R,3aS,5R,5aS,8aR)- (9CI)(615265-09-3)
EPA Substance Registry System: 2H,6H,8H-Difuro[3,2-b:3,4-c]furan-6-one, tetrahydro-3,5-dihydroxy-5-methyl-, (3R,3aS,5R,5aS,8aR)- (9CI)(615265-09-3)

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: 615265-09-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 615265-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,5,2,6 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 615265-09:
(8*6)+(7*1)+(6*5)+(5*2)+(4*6)+(3*5)+(2*0)+(1*9)=143
143 % 10 = 3
So 615265-09-3 is a valid CAS Registry Number.

615265-09-3Upstream product

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615265-09-3Relevant academic research and scientific papers

Factors controlling the biomimetic triple cyclisation of xylulose β-keto-esters to syringolides. Part 1: Synthesis of 4′-deoxysyringolide 2

Bennett, Simon A.,Rickards, Rodney W.

, p. 6927 - 6930 (2003)

Treatment of the 4-deoxy-D-xylulose β-ketodecanoate 13c with basic alumina affords 4′-deoxysyringolide 2 14 as a single stereoisomer, indicating that the course of the biomimetic triple cyclisation of the corresponding D-xylulose ester 3b to syringolide 2 5b is not dependent upon the presence of the 4R-hydroxyl group. The diacyl butanolide 15 is formed simultaneously by a side reaction of the initial Knoevenagel condensation product of the ester 13c.

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