Cas 499767-96-3,[1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-3-oxo-heptadec-4-enyl]-carbamic acid tert-butyl ester

499767-96-3

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Basic information

Product Name: [1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-3-oxo-heptadec-4-enyl]-carbamic acid tert-butyl ester
Synonyms: [1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-3-oxo-heptadec-4-enyl]-carbamic acid tert-butyl ester
CAS NO:499767-96-3
Molecular Formula:
Molecular Weight: 766.265
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: [1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-3-oxo-heptadec-4-enyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-3-oxo-heptadec-4-enyl]-carbamic acid tert-butyl ester(499767-96-3)
EPA Substance Registry System: [1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-3-oxo-heptadec-4-enyl]-carbamic acid tert-butyl ester(499767-96-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 499767-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 499767-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,7,6 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 499767-96:
(8*4)+(7*9)+(6*9)+(5*7)+(4*6)+(3*7)+(2*9)+(1*6)=253
253 % 10 = 3
So 499767-96-3 is a valid CAS Registry Number.

499767-96-3Upstream product

499767-96-3Downstream Products

499767-96-3Relevant academic research and scientific papers

Facile transformation of 2-azetidinones to unsaturated ketones: Application to the formal synthesis of sphingosine and phytosphingosine

Lee, Hyeon Kyu,Kim, Eun-Kyung,Pak, Chwang Siek

, p. 9641 - 9644 (2007/10/03)

2-Azetidinones were smoothly transformed to unsaturated ketones through the ring opening of activated 2-azetidinone by phosphonate stabilized carbanion and subsequent Horner-Wadsworth-Emmons olefination of the resulting β-ketophosphonates with aldehydes.

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