Cas 1429656-23-4,N-(2-(2-bromophenyl)-2-(naphthalen-1-yloxy)ethyl)-4-methylbenzenesulfonamide

1429656-23-4

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Basic information

Product Name: N-(2-(2-bromophenyl)-2-(naphthalen-1-yloxy)ethyl)-4-methylbenzenesulfonamide
Synonyms: N-(2-(2-bromophenyl)-2-(naphthalen-1-yloxy)ethyl)-4-methylbenzenesulfonamide
CAS NO:1429656-23-4
Molecular Formula:
Molecular Weight: 496.425
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-(2-(2-bromophenyl)-2-(naphthalen-1-yloxy)ethyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-(2-bromophenyl)-2-(naphthalen-1-yloxy)ethyl)-4-methylbenzenesulfonamide(1429656-23-4)
EPA Substance Registry System: N-(2-(2-bromophenyl)-2-(naphthalen-1-yloxy)ethyl)-4-methylbenzenesulfonamide(1429656-23-4)

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: 1429656-23-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1429656-23-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,6,5 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1429656-23:
(9*1)+(8*4)+(7*2)+(6*9)+(5*6)+(4*5)+(3*6)+(2*2)+(1*3)=184
184 % 10 = 4
So 1429656-23-4 is a valid CAS Registry Number.

1429656-23-4Upstream product

1429656-23-4Downstream Products

1429656-33-6 3-(naphthalen-1-yloxyl)-1-tosylindoline

1429656-23-4Relevant academic research and scientific papers

Synthetic route to chiral indolines via ring-opening/C-N cyclization of activated 2-haloarylaziridines

Ghorai, Manas K.,Nanaji

, p. 3867 - 3878 (2013/06/05)

A practical approach for the synthesis of 3-substituted indolines via regio- and stereoselective SN2-type ring-opening of 2-(2-halophenyl)-N-tosylaziridines with heteroatomic nucleophiles (O, N, and S) followed by palladium-catalyzed intramolecular C-N cyclization is reported in excellent yields (up to >99%) and enantiomeric excess (ee 99%).

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