Cas 609306-96-9,8-[(2R,3S)-2-(Benzyl-dimethyl-silanyl)-3-((R)-1-hydroxy-2-methyl-propyl)-oxiranyl]-octanoic acid methyl ester

609306-96-9

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Basic information

Product Name: 8-[(2R,3S)-2-(Benzyl-dimethyl-silanyl)-3-((R)-1-hydroxy-2-methyl-propyl)-oxiranyl]-octanoic acid methyl ester
Synonyms: 8-[(2R,3S)-2-(Benzyl-dimethyl-silanyl)-3-((R)-1-hydroxy-2-methyl-propyl)-oxiranyl]-octanoic acid methyl ester
CAS NO:609306-96-9
Molecular Formula:
Molecular Weight: 420.665
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: 8-[(2R,3S)-2-(Benzyl-dimethyl-silanyl)-3-((R)-1-hydroxy-2-methyl-propyl)-oxiranyl]-octanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 8-[(2R,3S)-2-(Benzyl-dimethyl-silanyl)-3-((R)-1-hydroxy-2-methyl-propyl)-oxiranyl]-octanoic acid methyl ester(609306-96-9)
EPA Substance Registry System: 8-[(2R,3S)-2-(Benzyl-dimethyl-silanyl)-3-((R)-1-hydroxy-2-methyl-propyl)-oxiranyl]-octanoic acid methyl ester(609306-96-9)

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: 609306-96-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 609306-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,9,3,0 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 609306-96:
(8*6)+(7*0)+(6*9)+(5*3)+(4*0)+(3*6)+(2*9)+(1*6)=159
159 % 10 = 9
So 609306-96-9 is a valid CAS Registry Number.

609306-96-9Upstream product

609306-96-9Downstream Products

609306-96-9Relevant academic research and scientific papers

Regioselective hydrosilylation of propargylic alcohols: An aldol surrogate

Trost, Barry M.,Ball, Zachary T.,Joege, Thomas

, p. 3415 - 3418 (2003)

Aldol products from a non-aldol reaction: A one-pot protocol effects hydrosilylation of propargyl alcohols and subsequent oxidative cleavage to yield β-hydroxy ketones in a chemo-, regio-, and enantioselective fashion. Further structural elaboration of th

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