Cas 284465-62-9,(R)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-pentanoic acid (R)-4,4-dimethyl-2-oxo-tetrahydro-furan-3-yl ester

284465-62-9

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Basic information

Product Name: (R)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-pentanoic acid (R)-4,4-dimethyl-2-oxo-tetrahydro-furan-3-yl ester
Synonyms:
CAS NO:284465-62-9
Molecular Formula:
Molecular Weight: 435.477
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)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-pentanoic acid (R)-4,4-dimethyl-2-oxo-tetrahydro-furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-pentanoic acid (R)-4,4-dimethyl-2-oxo-tetrahydro-furan-3-yl ester(284465-62-9)
EPA Substance Registry System: (R)-5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-pentanoic acid (R)-4,4-dimethyl-2-oxo-tetrahydro-furan-3-yl ester(284465-62-9)

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: 284465-62-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 284465-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,4,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 284465-62:
(8*2)+(7*8)+(6*4)+(5*4)+(4*6)+(3*5)+(2*6)+(1*2)=169
169 % 10 = 9
So 284465-62-9 is a valid CAS Registry Number.

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284465-62-9Relevant academic research and scientific papers

First asymmetric synthesis of (R)-(-)-α-phenyl δ-amino valeric acid

Calmes, Monique,Escale, Francoise,Juan, Emmanuelle,Rolland, Marc,Martinez, Jean

, p. 1263 - 1266 (2007/10/03)

An efficient synthesis of the (R)-(-)-α-phenyl δ-amino valeric acid 1 is described starting from commercially available compounds. The key intermediate in this synthesis is the corresponding totally protected prochiral ketene. (C) 2000 Elsevier Science Ltd.

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