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65486-33-1

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65486-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65486-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,8 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65486-33:
(7*6)+(6*5)+(5*4)+(4*8)+(3*6)+(2*3)+(1*3)=151
151 % 10 = 1
So 65486-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H17NO/c19-17-12-6-10-15-9-4-5-11-16(15)18(17)13-14-7-2-1-3-8-14/h1-5,7-9,11H,6,10,12-13H2

65486-33-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one

1.2 Other means of identification

Product number -
Other names N-benzyl-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65486-33-1 SDS

65486-33-1Downstream Products

65486-33-1Relevant articles and documents

Delineating ligand effects in intramolecular aryl amidation reactions: formation of a novel spiro-heterocycle by a tandem cyclisation process

Cropper, Emma L.,Yuen, Aui-Ping,Ford, Agnes,White, Andrew J.P.,(Mimi) Hii, King Kuok

experimental part, p. 525 - 530 (2009/04/07)

Ligand effects for intramolecular Pd-catalysed aryl amidation reaction were examined for the synthesis of seven-membered benzolactam rings. In an attempt to produce an eight-membered ring, tandem C-N/C-O bond forming reactions occurred to give a novel spi

The development of efficient protocols for the palladium-catalyzed cyclization reactions of secondary amides and carbamates

Yang, Bryant H.,Buchwald, Stephen L.

, p. 35 - 37 (2008/02/11)

(equation presented) With the proper choice of palladium catalyst, ligand, and base, five-, six-, and seven-membered rings are formed efficiently from secondary amide or secondary carbamate precursors, offering significant improvements to currently existing methodology.

Aryl radical cyclisations: Quinoline, isoquinolone, and 1-benzazepin-2-one rings via 6- and 7-exo cyclisations

Clark,Jones,McCarthy,Storey

, p. 2829 - 2832 (2007/10/02)

The cyclisation of aryl radicals derived by treatment of aryl halides (1a), (1b), (4), (7a), (7b), and (10) with tri-n-butyltin hydride has been investigated.

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