Cas 147555-69-9,(Z)-7-{(1S,5R,6S,7S)-7-[(E)-(R)-3-(tert-Butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-oxo-2,4-dioxa-bicyclo[3.2.1]oct-6-yl}-hept-5-enoic acid benzyl ester

147555-69-9

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Basic information

Product Name: (Z)-7-{(1S,5R,6S,7S)-7-[(E)-(R)-3-(tert-Butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-oxo-2,4-dioxa-bicyclo[3.2.1]oct-6-yl}-hept-5-enoic acid benzyl ester
Synonyms: (Z)-7-{(1S,5R,6S,7S)-7-[(E)-(R)-3-(tert-Butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-oxo-2,4-dioxa-bicyclo[3.2.1]oct-6-yl}-hept-5-enoic acid benzyl ester
CAS NO:147555-69-9
Molecular Formula:
Molecular Weight: 584.869
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: (Z)-7-{(1S,5R,6S,7S)-7-[(E)-(R)-3-(tert-Butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-oxo-2,4-dioxa-bicyclo[3.2.1]oct-6-yl}-hept-5-enoic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-7-{(1S,5R,6S,7S)-7-[(E)-(R)-3-(tert-Butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-oxo-2,4-dioxa-bicyclo[3.2.1]oct-6-yl}-hept-5-enoic acid benzyl ester(147555-69-9)
EPA Substance Registry System: (Z)-7-{(1S,5R,6S,7S)-7-[(E)-(R)-3-(tert-Butyl-dimethyl-silanyloxy)-oct-1-enyl]-3-oxo-2,4-dioxa-bicyclo[3.2.1]oct-6-yl}-hept-5-enoic acid benzyl ester(147555-69-9)

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: 147555-69-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147555-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,5 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147555-69:
(8*1)+(7*4)+(6*7)+(5*5)+(4*5)+(3*5)+(2*6)+(1*9)=159
159 % 10 = 9
So 147555-69-9 is a valid CAS Registry Number.

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147555-69-9Relevant academic research and scientific papers

A Safe and Efficient Method For Conversion of 1,2- and 1,3-Diols to Cyclic Carbonates Utilizing Triphosgene

Burk, Robert M.,Roof, Michael B.

, p. 395 - 398 (1993)

Reaction of triphosgene in the presence of pyridine with a variety of diols including hindered tertiary and 1,3-diols provided high yields of the corresponding cyclic carbonates.

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