Cas 359406-65-8,(E)-(5S,6R)-6-Benzyloxy-5-methyl-8-phenyl-oct-3-en-7-ynoic acid methyl ester

359406-65-8

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Basic information

Product Name: (E)-(5S,6R)-6-Benzyloxy-5-methyl-8-phenyl-oct-3-en-7-ynoic acid methyl ester
Synonyms: (E)-(5S,6R)-6-Benzyloxy-5-methyl-8-phenyl-oct-3-en-7-ynoic acid methyl ester
CAS NO:359406-65-8
Molecular Formula:
Molecular Weight: 348.442
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: (E)-(5S,6R)-6-Benzyloxy-5-methyl-8-phenyl-oct-3-en-7-ynoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(5S,6R)-6-Benzyloxy-5-methyl-8-phenyl-oct-3-en-7-ynoic acid methyl ester(359406-65-8)
EPA Substance Registry System: (E)-(5S,6R)-6-Benzyloxy-5-methyl-8-phenyl-oct-3-en-7-ynoic acid methyl ester(359406-65-8)

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: 359406-65-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 359406-65-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,4,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 359406-65:
(8*3)+(7*5)+(6*9)+(5*4)+(4*0)+(3*6)+(2*6)+(1*5)=168
168 % 10 = 8
So 359406-65-8 is a valid CAS Registry Number.

359406-65-8Upstream product

136314-66-4 methyl (3S,4E)-3-(dimethylphenylsilyl)-4-hexenoate

359406-65-8Downstream Products

359406-65-8Relevant academic research and scientific papers

Enhanced diastereoselectivity in asymmetric crotylation reactions using propargylic dicobalt hexacarbonyl complexes.

Sui,Panek

, p. 2439 - 2442 (2001)

[reaction: see text] Hexacarbonyl dicobalt complexes of propargylic acetals undergo Lewis acid catalyzed crotylation reactions with enhanced levels of diastereoselectivity (dr 6 to >20:1, syn/anti) while efficiently producing stereochemically well-defined

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