Cas 1242430-47-2,(R)-5-benzyl-1-((S)-2-hydroxy-1-(4-methoxyphenyl)ethyl)-4-methoxy-3-methyl-1H-pyrrol-2(5H)-one

1242430-47-2

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Basic information

Product Name: (R)-5-benzyl-1-((S)-2-hydroxy-1-(4-methoxyphenyl)ethyl)-4-methoxy-3-methyl-1H-pyrrol-2(5H)-one
Synonyms: (R)-5-benzyl-1-((S)-2-hydroxy-1-(4-methoxyphenyl)ethyl)-4-methoxy-3-methyl-1H-pyrrol-2(5H)-one
CAS NO:1242430-47-2
Molecular Formula:
Molecular Weight: 367.445
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-benzyl-1-((S)-2-hydroxy-1-(4-methoxyphenyl)ethyl)-4-methoxy-3-methyl-1H-pyrrol-2(5H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (R)-5-benzyl-1-((S)-2-hydroxy-1-(4-methoxyphenyl)ethyl)-4-methoxy-3-methyl-1H-pyrrol-2(5H)-one(1242430-47-2)
EPA Substance Registry System: (R)-5-benzyl-1-((S)-2-hydroxy-1-(4-methoxyphenyl)ethyl)-4-methoxy-3-methyl-1H-pyrrol-2(5H)-one(1242430-47-2)

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: 1242430-47-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242430-47-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,4,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1242430-47:
(9*1)+(8*2)+(7*4)+(6*2)+(5*4)+(4*3)+(3*0)+(2*4)+(1*7)=112
112 % 10 = 2
So 1242430-47-2 is a valid CAS Registry Number.

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1242430-47-2Relevant academic research and scientific papers

The first enantioselective synthesis of cytotoxic marine natural product palau'imide and assignment of its C-20 stereochemistry

Lan, Hong-Qiao,Ruan, Yuan-Ping,Huang, Pei-Qiang

supporting information; experimental part, p. 5319 - 5321 (2010/09/03)

Methyl tetramate derivative 6 has been developed as a new building block for the flexible and racemization-free synthesis of methyl 5-benzyl-3- methyltetramate via alkylation, and used in the first asymmetric synthesis of palau'imide (1). This allowed the establishment of the hitherto unknown stereochemistry at the C-20 of palau'imide as S.

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