Cas 940288-07-3,(3S,6R)-3-allyl-6-benzyloxymethyl-1-(2,4-dimethoxybenzyl)-4-iodo-3,6-dihydro-1H-pyridin-2-one

940288-07-3

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Basic information

Product Name: (3S,6R)-3-allyl-6-benzyloxymethyl-1-(2,4-dimethoxybenzyl)-4-iodo-3,6-dihydro-1H-pyridin-2-one
Synonyms: (3S,6R)-3-allyl-6-benzyloxymethyl-1-(2,4-dimethoxybenzyl)-4-iodo-3,6-dihydro-1H-pyridin-2-one
CAS NO:940288-07-3
Molecular Formula:
Molecular Weight: 533.406
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: (3S,6R)-3-allyl-6-benzyloxymethyl-1-(2,4-dimethoxybenzyl)-4-iodo-3,6-dihydro-1H-pyridin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,6R)-3-allyl-6-benzyloxymethyl-1-(2,4-dimethoxybenzyl)-4-iodo-3,6-dihydro-1H-pyridin-2-one(940288-07-3)
EPA Substance Registry System: (3S,6R)-3-allyl-6-benzyloxymethyl-1-(2,4-dimethoxybenzyl)-4-iodo-3,6-dihydro-1H-pyridin-2-one(940288-07-3)

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: 940288-07-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 940288-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,0,2,8 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 940288-07:
(8*9)+(7*4)+(6*0)+(5*2)+(4*8)+(3*8)+(2*0)+(1*7)=173
173 % 10 = 3
So 940288-07-3 is a valid CAS Registry Number.

940288-07-3Upstream product

72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

940288-07-3Downstream Products

940288-07-3Relevant academic research and scientific papers

Development of copper-mediated allylation of γ-activated-α,β-unsaturated lactam toward peptide mimetic synthesis

Sasaki, Yoshikazu,Yamaguchi, Keiko,Tsuji, Takashi,Shigenaga, Akira,Fujii, Nobutaka,Otaka, Akira

, p. 3221 - 3224 (2007/10/03)

Reactions of γ-activated-α,β-unsaturated lactams with allylboronate in the presence of LiOi-Pr and CuX (stoichiometric or catalytic amount) proceed in an anti-SN2′ manner to yield α-allylated compounds that serve as a potential synthetic interm

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