Cas 1202785-03-2,(R)-{4-[3-(allyloxy)hex-5-enyl]phenoxy}(tert-butyl)dimethylsilane

1202785-03-2

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Basic information

Product Name: (R)-{4-[3-(allyloxy)hex-5-enyl]phenoxy}(tert-butyl)dimethylsilane
Synonyms: (R)-{4-[3-(allyloxy)hex-5-enyl]phenoxy}(tert-butyl)dimethylsilane
CAS NO:1202785-03-2
Molecular Formula:
Molecular Weight: 346.585
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: (R)-{4-[3-(allyloxy)hex-5-enyl]phenoxy}(tert-butyl)dimethylsilane(CAS DataBase Reference)
NIST Chemistry Reference: (R)-{4-[3-(allyloxy)hex-5-enyl]phenoxy}(tert-butyl)dimethylsilane(1202785-03-2)
EPA Substance Registry System: (R)-{4-[3-(allyloxy)hex-5-enyl]phenoxy}(tert-butyl)dimethylsilane(1202785-03-2)

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: 1202785-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1202785-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,7,8 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1202785-03:
(9*1)+(8*2)+(7*0)+(6*2)+(5*7)+(4*8)+(3*5)+(2*0)+(1*3)=122
122 % 10 = 2
So 1202785-03-2 is a valid CAS Registry Number.

1202785-03-2Upstream product

106-95-6 allyl bromide

1202785-03-2Downstream Products

1202785-04-3 (S)-2-[4-(tert-butyldimethylsilyloxy)phenethyl]-3,4-dihydro-2H-pyran

1202785-03-2Relevant academic research and scientific papers

A stereodivergent synthesis of all stereoisomers of centrolobine: Control of selectivity by a protecting-group manipulation

Schmidt, Bernd,Hoelter, Frank

experimental part, p. 11948 - 11953 (2010/05/18)

All stereoisomers of the natural product centrolobine are selectively synthesized, by starting from a common precursor. Key steps are an enantioselective allylation with enantiomerically pure allylsilanes, a tandem ring-closing metathesis-isomerization re

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