Cas 357914-69-3,Acetic acid 3-(4-methoxy-phenyl)-1-((1R,2S)-1-phenethyl-2-trimethylsilanyl-but-3-enyloxy)-propyl ester

357914-69-3

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Basic information

Product Name: Acetic acid 3-(4-methoxy-phenyl)-1-((1R,2S)-1-phenethyl-2-trimethylsilanyl-but-3-enyloxy)-propyl ester
Synonyms:
CAS NO:357914-69-3
Molecular Formula:
Molecular Weight: 454.682
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: Acetic acid 3-(4-methoxy-phenyl)-1-((1R,2S)-1-phenethyl-2-trimethylsilanyl-but-3-enyloxy)-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 3-(4-methoxy-phenyl)-1-((1R,2S)-1-phenethyl-2-trimethylsilanyl-but-3-enyloxy)-propyl ester(357914-69-3)
EPA Substance Registry System: Acetic acid 3-(4-methoxy-phenyl)-1-((1R,2S)-1-phenethyl-2-trimethylsilanyl-but-3-enyloxy)-propyl ester(357914-69-3)

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: 357914-69-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 357914-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,9,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 357914-69:
(8*3)+(7*5)+(6*7)+(5*9)+(4*1)+(3*4)+(2*6)+(1*9)=183
183 % 10 = 3
So 357914-69-3 is a valid CAS Registry Number.

357914-69-3Upstream product

357914-69-3Downstream Products

357914-69-3Relevant academic research and scientific papers

Studies on the synthesis of 2,6-disubstituted dihydropyrans: Intervention of oxonia-cope rearrangements in the lewis acid mediated cyclodehydrative reactions of aldehydes and β-hydroxyallylsilanes

Roush,Dilley

, p. 955 - 959 (2007/10/03)

The dehydrative coupling reactions of anti-β-hydroxyallylsilanes 5 and aldehydes provide 2,6-cis-dihydropyrans 27 by pathways involving oxonium ions that cyclize via boat-like transition state 21, with the intervention of oxonia-Cope rearrangements (21 → 29).

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