Cas 851786-79-3,Silane, (1,1-dimethylethyl)dimethyl[[1-[(phenylmethoxy)methyl]-4-pentenyl]oxy]-

851786-79-3

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Basic information

Product Name: Silane, (1,1-dimethylethyl)dimethyl[[1-[(phenylmethoxy)methyl]-4-pentenyl]oxy]-
Synonyms:
CAS NO:851786-79-3
Molecular Formula: C19H32O2Si
Molecular Weight: 320.547
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: Silane, (1,1-dimethylethyl)dimethyl[[1-[(phenylmethoxy)methyl]-4-pentenyl]oxy]-(CAS DataBase Reference)
NIST Chemistry Reference: Silane, (1,1-dimethylethyl)dimethyl[[1-[(phenylmethoxy)methyl]-4-pentenyl]oxy]-(851786-79-3)
EPA Substance Registry System: Silane, (1,1-dimethylethyl)dimethyl[[1-[(phenylmethoxy)methyl]-4-pentenyl]oxy]-(851786-79-3)

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: 851786-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 851786-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,7,8 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 851786-79:
(8*8)+(7*5)+(6*1)+(5*7)+(4*8)+(3*6)+(2*7)+(1*9)=213
213 % 10 = 3
So 851786-79-3 is a valid CAS Registry Number.

851786-79-3Upstream product

851786-79-3Downstream Products

851786-79-3Relevant academic research and scientific papers

New functionalised hydroxymethyl ketones from the mild and chemoselective KMnO4 oxidation of chiral terminal olefins

Bonini, Carlo,Chiummiento, Lucia,Funicello, Maria,Lupattelli, Paolo,Pullez, Maddalena

, p. 80 - 83 (2006)

Various terminal olefinic compounds are directly converted into the corresponding α-hydroxy ketones in good yields by potassium permanganate oxidation. The reaction is also highly chemoselective in the presence of differently protected hydroxy groups and

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