Cas 1315506-41-2,N-(2-((6-bromobenzo[d][1,3]dioxol-5-yl)(cyano)methyl)cyclopentyl)-4-methylbenzenesulfonamide

1315506-41-2

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Basic information

Product Name: N-(2-((6-bromobenzo[d][1,3]dioxol-5-yl)(cyano)methyl)cyclopentyl)-4-methylbenzenesulfonamide
Synonyms: N-(2-((6-bromobenzo[d][1,3]dioxol-5-yl)(cyano)methyl)cyclopentyl)-4-methylbenzenesulfonamide
CAS NO:1315506-41-2
Molecular Formula:
Molecular Weight: 477.379
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-((6-bromobenzo[d][1,3]dioxol-5-yl)(cyano)methyl)cyclopentyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-((6-bromobenzo[d][1,3]dioxol-5-yl)(cyano)methyl)cyclopentyl)-4-methylbenzenesulfonamide(1315506-41-2)
EPA Substance Registry System: N-(2-((6-bromobenzo[d][1,3]dioxol-5-yl)(cyano)methyl)cyclopentyl)-4-methylbenzenesulfonamide(1315506-41-2)

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: 1315506-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1315506-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1315506-41:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*0)+(3*6)+(2*4)+(1*1)=122
122 % 10 = 2
So 1315506-41-2 is a valid CAS Registry Number.

1315506-41-2Upstream product

1315506-41-2Downstream Products

1315506-47-8 5-tosyl-5a,6,7,8,8a,9-hexahydro-5H-cyclopenta[b][1,3]dioxolo[4,5-g]quinoline-9-carbonitile

1315506-41-2Relevant academic research and scientific papers

Ring opening/C-N cyclization of activated aziridines with carbon nucleophiles: Highly diastereo- and enantioselective synthesis of tetrahydroquinolines

Ghorai, Manas K.,Nanaji,Yadav

supporting information; experimental part, p. 4256 - 4259 (2011/10/08)

A simple strategy for the synthesis of substituted tetrahydroquinolines through regio- and stereoselective ring opening of N-tosyl aziridines with carbon nucleophiles generated from 2-(bromoaryl)acetonitriles followed by palladium-catalyzed intramolecular

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