Cas 1228675-52-2,tert-butyl(((3S,4R)-1-((4-methoxybenzyl)oxy)-4-methyl-8-(trimethylsilyl)oct-7-yn-3-yl)oxy)dimethylsilane

1228675-52-2

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Basic information

Product Name: tert-butyl(((3S,4R)-1-((4-methoxybenzyl)oxy)-4-methyl-8-(trimethylsilyl)oct-7-yn-3-yl)oxy)dimethylsilane
Synonyms: tert-butyl(((3S,4R)-1-((4-methoxybenzyl)oxy)-4-methyl-8-(trimethylsilyl)oct-7-yn-3-yl)oxy)dimethylsilane
CAS NO:1228675-52-2
Molecular Formula:
Molecular Weight: 462.82
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: tert-butyl(((3S,4R)-1-((4-methoxybenzyl)oxy)-4-methyl-8-(trimethylsilyl)oct-7-yn-3-yl)oxy)dimethylsilane(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl(((3S,4R)-1-((4-methoxybenzyl)oxy)-4-methyl-8-(trimethylsilyl)oct-7-yn-3-yl)oxy)dimethylsilane(1228675-52-2)
EPA Substance Registry System: tert-butyl(((3S,4R)-1-((4-methoxybenzyl)oxy)-4-methyl-8-(trimethylsilyl)oct-7-yn-3-yl)oxy)dimethylsilane(1228675-52-2)

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: 1228675-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1228675-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,6,7 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1228675-52:
(9*1)+(8*2)+(7*2)+(6*8)+(5*6)+(4*7)+(3*5)+(2*5)+(1*2)=172
172 % 10 = 2
So 1228675-52-2 is a valid CAS Registry Number.

1228675-52-2Upstream product

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1228675-52-2Relevant academic research and scientific papers

Polyketide assembly by alkene-alkyne reductive cross-coupling: Spiroketals through the union of homoallylic alcohols

Canterbury, Daniel P.,Micalizio, Glenn C.

, p. 7602 - 7604 (2010)

A reaction sequence composed of regioselective formal hydroalkynylation, reductive ene-yne cross-coupling, and oxidative cyclization has been developed to prepare stereochemically dense spiroketals. Overall, the chemistry defines a three-component coupling process for the union of two homoallylic alcohol-based substrates with trimethylsilylacetylene.

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