Cas 353466-97-4,1-benzyl-3-[2-(2-furyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one

353466-97-4

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Basic information

Product Name: 1-benzyl-3-[2-(2-furyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one
Synonyms: 1-benzyl-3-[2-(2-furyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one
CAS NO:353466-97-4
Molecular Formula: C21H17NO4
Molecular Weight: 347.36398
EINECS: N/A
Product Categories: N/A
Mol File: 353466-97-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-benzyl-3-[2-(2-furyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyl-3-[2-(2-furyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one(353466-97-4)
EPA Substance Registry System: 1-benzyl-3-[2-(2-furyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one(353466-97-4)

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: 353466-97-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 353466-97-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,4,6 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 353466-97:
(8*3)+(7*5)+(6*3)+(5*4)+(4*6)+(3*6)+(2*9)+(1*7)=164
164 % 10 = 4
So 353466-97-4 is a valid CAS Registry Number.

353466-97-4Upstream product

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353466-97-4Relevant academic research and scientific papers

Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo- and Enantioconvergent Michael–Henry Reactions to Afford Spirooxindoles Bearing Furan-Fused Rings

Sohail, Muhammad,Tanaka, Fujie

, (2021)

Dynamic kinetic asymmetric transformation (DYKAT) reactions of racemic diastereomer mixtures that afford the products as essentially single diastereomers with high enantioselectivities are described. We demonstrated the DYKAT in the diastereo- and enantio

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