Cas 207281-59-2,(4R,5S)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-6-phenyl-hexanoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

207281-59-2

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Basic information

Product Name: (4R,5S)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-6-phenyl-hexanoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms: (4R,5S)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-6-phenyl-hexanoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
CAS NO:207281-59-2
Molecular Formula:
Molecular Weight: 491.627
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: (4R,5S)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-6-phenyl-hexanoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5S)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-6-phenyl-hexanoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(207281-59-2)
EPA Substance Registry System: (4R,5S)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-6-phenyl-hexanoic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(207281-59-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 207281-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 207281-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,2,8 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 207281-59:
(8*2)+(7*0)+(6*7)+(5*2)+(4*8)+(3*1)+(2*5)+(1*9)=122
122 % 10 = 2
So 207281-59-2 is a valid CAS Registry Number.

207281-59-2Upstream product

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207281-59-2Relevant academic research and scientific papers

A General, Catalytic, and Enantioselective Synthesis of (S)-γ-[(S)-1-Aminoalkyl]-γ-lactones

Aguilar, Núria,Moyano, Albert,Pericàs, Miquel A.,Riera, Antoni

, p. 3560 - 3567 (1998)

A catalytic asymmetric synthesis of N-phthaloyl (S)-γ-[(S)-1-aminoalkyl]-γ-lactones, widely used intermediates in the preparation of hydroxyethylene dipeptide isosteres, is described. The highly enantiopure epoxy alcohols arising from the Sharpless epoxid

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