Cas 1208882-53-4,N-((2R,3R)-2-hydroxy-3-isopropyl-2,3-dihydronaphtho[1,2-b]furan-5-yl)-4-methylbenzenesulfonamide

1208882-53-4

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Basic information

Product Name: N-((2R,3R)-2-hydroxy-3-isopropyl-2,3-dihydronaphtho[1,2-b]furan-5-yl)-4-methylbenzenesulfonamide
Synonyms: N-((2R,3R)-2-hydroxy-3-isopropyl-2,3-dihydronaphtho[1,2-b]furan-5-yl)-4-methylbenzenesulfonamide
CAS NO:1208882-53-4
Molecular Formula:
Molecular Weight: 397.495
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: N-((2R,3R)-2-hydroxy-3-isopropyl-2,3-dihydronaphtho[1,2-b]furan-5-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((2R,3R)-2-hydroxy-3-isopropyl-2,3-dihydronaphtho[1,2-b]furan-5-yl)-4-methylbenzenesulfonamide(1208882-53-4)
EPA Substance Registry System: N-((2R,3R)-2-hydroxy-3-isopropyl-2,3-dihydronaphtho[1,2-b]furan-5-yl)-4-methylbenzenesulfonamide(1208882-53-4)

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: 1208882-53-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1208882-53-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,8,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1208882-53:
(9*1)+(8*2)+(7*0)+(6*8)+(5*8)+(4*8)+(3*2)+(2*5)+(1*3)=164
164 % 10 = 4
So 1208882-53-4 is a valid CAS Registry Number.

1208882-53-4Upstream product

590-86-3 isovaleraldehyde

1208882-53-4Downstream Products

1208882-70-5 (R)-N-(4-hydroxy-3-(1-hydroxy-3-methylbutan-2-yl)naphthalen-1-yl)-4-methylbenzenesulfonamide

1208882-53-4Relevant academic research and scientific papers

Anodic oxidation and organocatalysis: Direct regio- And stereo-selective access to meta-substituted anilines by α-arylation of aldehydes

Jensen, Kim L.,Franke, Patrick T.,Nielsen, Lasse T.,Daasbjerg, Kim,Jorgensen, Karl Anker

supporting information; experimental part, p. 129 - 133 (2010/03/30)

(Figure presented) What's the potential? An anodic oxidation/ organocatalytic α-arylation of aldehydes using substituted electron-rich aromatic compounds has been developed. The method gives access to meta-substituted anilines and dihydrobenzofurans in go

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