Cas 204650-71-5,3-Oxo-dec-9-enoic acid (3aS,6R,6aS)-6-hydroxy-2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethyl ester

204650-71-5

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Basic information

Product Name: 3-Oxo-dec-9-enoic acid (3aS,6R,6aS)-6-hydroxy-2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethyl ester
Synonyms:
CAS NO:204650-71-5
Molecular Formula:
Molecular Weight: 434.486
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: 3-Oxo-dec-9-enoic acid (3aS,6R,6aS)-6-hydroxy-2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Oxo-dec-9-enoic acid (3aS,6R,6aS)-6-hydroxy-2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethyl ester(204650-71-5)
EPA Substance Registry System: 3-Oxo-dec-9-enoic acid (3aS,6R,6aS)-6-hydroxy-2-(4-methoxy-phenyl)-dihydro-furo[2,3-d][1,3]dioxol-3a-ylmethyl ester(204650-71-5)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 204650-71-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 204650-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,6,5 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 204650-71:
(8*2)+(7*0)+(6*4)+(5*6)+(4*5)+(3*0)+(2*7)+(1*1)=105
105 % 10 = 5
So 204650-71-5 is a valid CAS Registry Number.

204650-71-5Upstream product

204650-71-5Downstream Products

204650-71-5Relevant academic research and scientific papers

Synthesis of the microbial elicitor syringolide 2 multiply labelled with deuterium

Henschke, Julian P.,Rickards, Rodney W.

, p. 211 - 220 (1998)

Multiply-deuterated syringolide 2 3 was prepared from D-xylulose and 8- bromooctanoic acid by a convergent route based on our previously reported biomimetic synthesis of this microbial elicitor. Key steps were the thermal acylation of the anisylidene-prot

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