Cas 1632036-73-7,(R)-2-[(1S,2R)-1-hydroxy-2-(methoxymethoxy)-2-phenylethyl]cyclopentanone

1632036-73-7

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Basic information

Product Name: (R)-2-[(1S,2R)-1-hydroxy-2-(methoxymethoxy)-2-phenylethyl]cyclopentanone
Synonyms: (R)-2-[(1S,2R)-1-hydroxy-2-(methoxymethoxy)-2-phenylethyl]cyclopentanone
CAS NO:1632036-73-7
Molecular Formula:
Molecular Weight: 264.321
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: (R)-2-[(1S,2R)-1-hydroxy-2-(methoxymethoxy)-2-phenylethyl]cyclopentanone(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-[(1S,2R)-1-hydroxy-2-(methoxymethoxy)-2-phenylethyl]cyclopentanone(1632036-73-7)
EPA Substance Registry System: (R)-2-[(1S,2R)-1-hydroxy-2-(methoxymethoxy)-2-phenylethyl]cyclopentanone(1632036-73-7)

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: 1632036-73-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1632036-73-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,3,2,0,3 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1632036-73:
(9*1)+(8*6)+(7*3)+(6*2)+(5*0)+(4*3)+(3*6)+(2*7)+(1*3)=137
137 % 10 = 7
So 1632036-73-7 is a valid CAS Registry Number.

1632036-73-7Upstream product

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1632036-73-7Relevant academic research and scientific papers

Synthesis of 7- Epi -goniodiol by proline-catalyzed diastereoselective direct aldol reaction

Veena, Bacchu,Sharma, Gangavaram V. M.

, p. 1283 - 1286 (2014)

A simple organocatalytic approach was developed for the total synthesis of 7-epi-goniodiol. The strategy involves l-proline-catalyzed diastereoselective direct aldol reaction and Baeyer-Villiger oxidation as key steps for the construction of chiral lactone. Georg Thieme Verlag Stuttgart New York.

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