Cas 78535-74-7,[(1R,4S)-2-Benzyloxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyloxy]-tert-butyl-dimethyl-silane

78535-74-7

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Basic information

Product Name: [(1R,4S)-2-Benzyloxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyloxy]-tert-butyl-dimethyl-silane
Synonyms: [(1R,4S)-2-Benzyloxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyloxy]-tert-butyl-dimethyl-silane
CAS NO:78535-74-7
Molecular Formula:
Molecular Weight: 418.649
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: [(1R,4S)-2-Benzyloxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyloxy]-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: [(1R,4S)-2-Benzyloxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyloxy]-tert-butyl-dimethyl-silane(78535-74-7)
EPA Substance Registry System: [(1R,4S)-2-Benzyloxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyloxy]-tert-butyl-dimethyl-silane(78535-74-7)

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: 78535-74-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78535-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,3 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78535-74:
(7*7)+(6*8)+(5*5)+(4*3)+(3*5)+(2*7)+(1*4)=167
167 % 10 = 7
So 78535-74-7 is a valid CAS Registry Number.

78535-74-7Upstream product

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78535-74-7Relevant academic research and scientific papers

CYCLOPENTANOIDS FROM PHENOL. PART VII. PREPARATION AND REACTIONS OF A 3-HYDROXY-5-OXOCYCLOPENT-1-ENYL CARBANION EQUIVALENT

Gill, Melvyn,Bainton, Paul,Rickards, Rodney W.

, p. 1437 - 1440 (2007/10/02)

(3S*,5R*)-1-Lithio-5-(t-butyldimethylsilyloxy)-3-(tetrahydropyran-2-yloxy)cyclopent-1-ene (7) is prepared from phenol via the chlorocyclopentenone (1) and the stannylcyclopentenl derivative (6); this latent 3-hydroxy-5-oxocyclopent-1

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