Cas 114143-87-2,((2R,3S,4S)-4-Allyl-2-ethyl-1-hydroxy-3,4-diphenyl-azetidin-2-yl)-((S)-2-methoxymethyl-pyrrolidin-1-yl)-methanone

114143-87-2

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Basic information

Product Name: ((2R,3S,4S)-4-Allyl-2-ethyl-1-hydroxy-3,4-diphenyl-azetidin-2-yl)-((S)-2-methoxymethyl-pyrrolidin-1-yl)-methanone
Synonyms: ((2R,3S,4S)-4-Allyl-2-ethyl-1-hydroxy-3,4-diphenyl-azetidin-2-yl)-((S)-2-methoxymethyl-pyrrolidin-1-yl)-methanone
CAS NO:114143-87-2
Molecular Formula:
Molecular Weight: 434.579
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: ((2R,3S,4S)-4-Allyl-2-ethyl-1-hydroxy-3,4-diphenyl-azetidin-2-yl)-((S)-2-methoxymethyl-pyrrolidin-1-yl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,3S,4S)-4-Allyl-2-ethyl-1-hydroxy-3,4-diphenyl-azetidin-2-yl)-((S)-2-methoxymethyl-pyrrolidin-1-yl)-methanone(114143-87-2)
EPA Substance Registry System: ((2R,3S,4S)-4-Allyl-2-ethyl-1-hydroxy-3,4-diphenyl-azetidin-2-yl)-((S)-2-methoxymethyl-pyrrolidin-1-yl)-methanone(114143-87-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 114143-87-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114143-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,4 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114143-87:
(8*1)+(7*1)+(6*4)+(5*1)+(4*4)+(3*3)+(2*8)+(1*7)=92
92 % 10 = 2
So 114143-87-2 is a valid CAS Registry Number.

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114143-87-2Relevant academic research and scientific papers

CHIRAL FOUR-MEMBERED CYCLIC NITRONES; ASYMETRIC INDUCTION IN THE (4+2)-CYCLOADDITION REACTION OF CHIRAL YNAMINES AND NITROALKENES

Elburg, P. A. van,Honing, G. W. N.,Reinhoudt, D. N.

, p. 6397 - 6400 (2007/10/02)

Chiral four-membered cyclic nitrones were synthesized by the asymmetric (4+2)-cycloaddition of nitroalkenes 1 and chiral ynamines 2.The subsequent stereoselective addition of nucleophiles to these nitrones enabled the synthesis of chiral N-hydroxyazetidines.

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