Cas 607405-54-9,(1S,2S,4S,5R)-2-[3-(benzyloxy)propyl]-4,7,7-trimethyl-5-[(tetrahydro-2H-pyran-2-yl)oxy]bicyclo[2.2.1]heptan-2-ol

607405-54-9

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Basic information

Product Name: (1S,2S,4S,5R)-2-[3-(benzyloxy)propyl]-4,7,7-trimethyl-5-[(tetrahydro-2H-pyran-2-yl)oxy]bicyclo[2.2.1]heptan-2-ol
Synonyms: (1S,2S,4S,5R)-2-[3-(benzyloxy)propyl]-4,7,7-trimethyl-5-[(tetrahydro-2H-pyran-2-yl)oxy]bicyclo[2.2.1]heptan-2-ol
CAS NO:607405-54-9
Molecular Formula:
Molecular Weight: 402.574
EINECS: N/A
Product Categories: N/A
Mol File: 607405-54-9.mol
Article Data: 1

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,2S,4S,5R)-2-[3-(benzyloxy)propyl]-4,7,7-trimethyl-5-[(tetrahydro-2H-pyran-2-yl)oxy]bicyclo[2.2.1]heptan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,4S,5R)-2-[3-(benzyloxy)propyl]-4,7,7-trimethyl-5-[(tetrahydro-2H-pyran-2-yl)oxy]bicyclo[2.2.1]heptan-2-ol(607405-54-9)
EPA Substance Registry System: (1S,2S,4S,5R)-2-[3-(benzyloxy)propyl]-4,7,7-trimethyl-5-[(tetrahydro-2H-pyran-2-yl)oxy]bicyclo[2.2.1]heptan-2-ol(607405-54-9)

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: 607405-54-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 607405-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,4,0 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 607405-54:
(8*6)+(7*0)+(6*7)+(5*4)+(4*0)+(3*5)+(2*5)+(1*4)=139
139 % 10 = 9
So 607405-54-9 is a valid CAS Registry Number.

607405-54-9Upstream product

5375-00-8 3-benzyloxypropyl iodide

607405-54-9Downstream Products

607405-54-9Relevant articles and documents

Total synthesis of dumsin. 1. Retrosynthetic strategy and the elaboration of key intermediates from (-)-bornyl acetate

Paquette, Leo A.,Hong, Fang-Tsao

, p. 6905 - 6918 (2007/10/03)

An intramolecular anionic oxy-Cope rearrangement (44 → 46) serves as the key step in a synthetic approach to the insect antifeedant dumsin. Initial investigations clarified the manner in which (-)-bornyl acetate may be transformed into the exo-norbornenol

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