Cas 128758-88-3,(S)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-(4-methoxy-benzyl)-3,4-dihydro-2H-isoquinolin-1-one

128758-88-3

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Basic information

Product Name: (S)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-(4-methoxy-benzyl)-3,4-dihydro-2H-isoquinolin-1-one
Synonyms:
CAS NO:128758-88-3
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: (S)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-(4-methoxy-benzyl)-3,4-dihydro-2H-isoquinolin-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-(4-methoxy-benzyl)-3,4-dihydro-2H-isoquinolin-1-one(128758-88-3)
EPA Substance Registry System: (S)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-(4-methoxy-benzyl)-3,4-dihydro-2H-isoquinolin-1-one(128758-88-3)

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: 128758-88-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128758-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,7,5 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 128758-88:
(8*1)+(7*2)+(6*8)+(5*7)+(4*5)+(3*8)+(2*8)+(1*8)=173
173 % 10 = 3
So 128758-88-3 is a valid CAS Registry Number.

128758-88-3Upstream product

128741-79-7 (3S,4S)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-(4-methoxy-benzyl)-1-oxo-1,2,3,4-tetrahydro-isoquinoline-4-carboxylic acid methyl ester

128758-88-3Downstream Products

128758-88-3Relevant academic research and scientific papers

Chelation control in the addition of homophthalic anhydride to α-alkoxy imines. Pancratistatin model studies

Clark, Robin D.,Souchet, Michel

, p. 193 - 196 (1990)

Diastereoselectivity in the addition of homophthalic anhydride to the α-alkoxy imine (S)-5 can be increased dramatically (to> 90%) with addition of Lewis acids. This methodology has been applied to the synthesis of a model compound (12) which contains four asymmetric centers with the same relative stereochemistry as pancratistatin (1).

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