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Bicyclo[3.3.1]non-6-en-3-one, 7-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

168984-32-5

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168984-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168984-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,9,8 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 168984-32:
(8*1)+(7*6)+(6*8)+(5*9)+(4*8)+(3*4)+(2*3)+(1*2)=195
195 % 10 = 5
So 168984-32-5 is a valid CAS Registry Number.

168984-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylbicyclo[3.3.1]non-3-en-7-one

1.2 Other means of identification

Product number -
Other names Bicyclo[3.3.1]non-6-en-3-one,7-phenyl

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:168984-32-5 SDS

168984-32-5Downstream Products

168984-32-5Relevant academic research and scientific papers

Synthesis of 2-oxaadamantane and 1-aryl-2-oxaadamantanes

Benneche, Tore,Tius, Marcus A.

, p. 3150 - 3151 (2016/07/06)

The direct reduction of 1-hydroxy-2-oxaadamantanes derivatives to give 2-oxaadamantanes was unsuccessful. 2-Oxaadamantanes could, however, be prepared from 1-hydroxy-2-oxaadamantes by a ring-opening reaction followed by reduction and subsequent ring-closu

Synthesis and pharmacological evaluation of (2-oxaadamant-1-yl)amines

Duque, Maria D.,Camps, Pelayo,Profire, Lenuta,Montaner, Silvia,Vazquez, Santiago,Sureda, Francesc X.,Mallol, Jordi,Lopez-Querol, Marta,Naesens, Lieve,Clercq, Erik De,Radhika Prathalingam,Kelly, John M.

scheme or table, p. 3198 - 3206 (2009/09/27)

The synthesis of several (2-oxaadamant-1-yl)amines is reported. They were evaluated as NMDA receptor antagonists and several of them were more active than amantadine, but none was more potent than memantine. None of the tested compounds displayed antivira

Easy synthesis of 7-alkylbicyclo[3.3.1]non-6-en-3-ones by silica gelpromoted fragmentation of 3-alkyl-2-oxaadamant-1-yl mesylates

Camps, Pelayo,El Achab, Rachid,Font-Bardia, Merce,Goerbig, Diana,Morral, Jordi,Munoz-Torrero, Diego,Solans, Xavier,Simon, Montserrat

, p. 5867 - 5880 (2007/10/03)

A synthesis of 7-alkylbicyclo[3.3.1]non-6-en-3-ones 4b-f and 4j,k by reaction of the corresponding 3-alkyl-2-oxaadamant-1-yl mesylates 3 with silica gel in methylene chloride at room temperature, is described. The method failed to give enones 4a,g and the

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