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Tricyclo[8.2.1.03,8]trideca-3,5,7-trien-13-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54962-18-4

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54962-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54962-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,6 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54962-18:
(7*5)+(6*4)+(5*9)+(4*6)+(3*2)+(2*1)+(1*8)=144
144 % 10 = 4
So 54962-18-4 is a valid CAS Registry Number.

54962-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Tricyclo[8.2.1.03,8]trideca-3,5,7-trien-13-one

1.2 Other means of identification

Product number -
Other names 11-oxo-5,6,7,8,9,10-hexahydro-6,9-methanobenzocyclooctene

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:54962-18-4 SDS

54962-18-4Relevant academic research and scientific papers

Synthesis and Reactions of 2,3,5,6-Tetrahydro-2,5-ethano-3-benzazocin-4(1H)-one and a Thieno-extended Analogue: X-Ray Structure of 3-Methyl-2,3,5,6-tetrahydro-2,5-ethanobenzothienoazocin-4(1H)-one

Iddon, Brian,Redhouse, Alan D.,Yat, Patrick N.

, p. 1083 - 1090 (2007/10/02)

5,6,7,8,9,10-Hexahydro-6,9-methanobenzocyclo-octen-11-one (3) was prepared through condensation of o-xylene-α,α'-diyl dibromide with N-cyclopentylidenepyrrolidine and converted by Beckmann rearrangement of its oxime (4) into 2,3,5,6-tetrahydro-2,5-ethano-3-benzazocin-4(1H)-one (6). 2,3-Bis(bromomethyl)benzothiophene was converted similarly into a mixture of 1,4,5,6-tetrahydro-2,5-ethanobenzothienoazocin-3(2H)-one (15) and the isomeric lactam (19).Lactam (6) was N-methylated and both the parent lactam (6) and the N-methyl derivative (23) were reducedwith lithium aluminium hydride to the saturated products (24) and (25), respectively.Conversion of lactam (6) into the corresponding thiolactam (26) with phosphorus pentasulphide followed by alkylation of the latter compound gave an N-(29) or S-alkylated derivative, (27) or (28), depending on the reagent and reaction conditions.Similar reactions are reported also for lactams (15) and (19).The 4(1H)-one structures of compounds (15) - (22) are based on an X-ray analysis of 3-methyl-2,3,5,6-tetrahydro-2,5-ethanobenzothienoazocin-4(1H)-one (20).We also report syntheses of 2-azido-5,6,7,8,9,10-hexahydro-6,9-methanobenzocyclo-octen-11-one (33) and 3-nitro(and 1,3-dinitro)-6,7,8,9,10,11-hexahydro-7,10-methanocyclo-octabenzothiophen-12-one, (36) and (37), respectively.

Derivatives of 2-hydroxy-6,9-methano-11-amino-5,6,7,8,9,10-hexahydro-benzocyclooctene

-

, (2008/06/13)

Novel amino derivatives of 2-hydroxy-6,9-methano-11-amino-5,6,7,8,9,10-hexahydro-benzocyclooctenes, methods for their preparation, and their use as effective analgesic agents is described.

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