Cas 174848-54-5,[(1S,3S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-pent-4-enyl]-carbamic acid benzyl ester

174848-54-5

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Basic information

Product Name: [(1S,3S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-pent-4-enyl]-carbamic acid benzyl ester
Synonyms:
CAS NO:174848-54-5
Molecular Formula:
Molecular Weight: 379.572
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: [(1S,3S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-pent-4-enyl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(1S,3S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-pent-4-enyl]-carbamic acid benzyl ester(174848-54-5)
EPA Substance Registry System: [(1S,3S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-pent-4-enyl]-carbamic acid benzyl ester(174848-54-5)

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: 174848-54-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 174848-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,8,4 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 174848-54:
(8*1)+(7*7)+(6*4)+(5*8)+(4*4)+(3*8)+(2*5)+(1*4)=175
175 % 10 = 5
So 174848-54-5 is a valid CAS Registry Number.

174848-54-5Upstream product

174848-54-5Downstream Products

1053271-26-3 C₂₈H₃₉NO₅SeSi

174848-54-5Relevant academic research and scientific papers

New methodology for the synthesis of unsaturated 8-, 9- and 10-membered lactams

Evans, P. Andrew,Holmes, Andrew B.,McGeary, Ross P.,Nadin, Alan,Russell, Keith,O'Hanlon, Peter J.,Pearson, Neil D.

, p. 123 - 138 (1996)

Unsaturated 8-, 9- and 10-membered medium ring lactams 1 (n = 1, 2, 3) have been prepared in good yield by the Claisen rearrangement of the vinyl-substituted precursors 3 in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).

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