Cas 1065253-15-7,(3S)-3-(2-(benzyloxy)ethyl)-2-(3-methoxy-5-methylphenyl)-3-methylcyclopentanone

1065253-15-7

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Basic information

Product Name: (3S)-3-(2-(benzyloxy)ethyl)-2-(3-methoxy-5-methylphenyl)-3-methylcyclopentanone
Synonyms: (3S)-3-(2-(benzyloxy)ethyl)-2-(3-methoxy-5-methylphenyl)-3-methylcyclopentanone
CAS NO:1065253-15-7
Molecular Formula:
Molecular Weight: 352.474
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: (3S)-3-(2-(benzyloxy)ethyl)-2-(3-methoxy-5-methylphenyl)-3-methylcyclopentanone(CAS DataBase Reference)
NIST Chemistry Reference: (3S)-3-(2-(benzyloxy)ethyl)-2-(3-methoxy-5-methylphenyl)-3-methylcyclopentanone(1065253-15-7)
EPA Substance Registry System: (3S)-3-(2-(benzyloxy)ethyl)-2-(3-methoxy-5-methylphenyl)-3-methylcyclopentanone(1065253-15-7)

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: 1065253-15-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1065253-15-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,5,2,5 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1065253-15:
(9*1)+(8*0)+(7*6)+(6*5)+(5*2)+(4*5)+(3*3)+(2*1)+(1*5)=127
127 % 10 = 7
So 1065253-15-7 is a valid CAS Registry Number.

1065253-15-7Upstream product

1065253-12-4 (5R)-7-(benzyloxy)-1-(3-methoxy-5-methylphenyl)-5-methyl-1-diazoheptan-2-one

1065253-15-7Downstream Products

1065253-26-0 (3S)-3-(2-hydroxyethyl)-2-(3-methoxy-5-methylphenyl)-3-methylcyclopentanone

1065253-15-7Relevant academic research and scientific papers

Synthesis of (-)-hamigeran B

Taber, Douglass F.,Tian, Weiwei

, p. 7560 - 7564 (2008)

(Chemical Equation Presented) The synthesis of (-)-hamigeran B has been achieved, based on a new approach to cyclopentane construction, the rhodium-mediated intramolecular C-H insertion of α-aryl-α- diazoketones. The endo- isopropyl group was installed by selective hydrogenation of a cyclopropylidene substituent.

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