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9-Azabicyclo[3.3.1]nonan-3-one, 1-pentyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51856-96-3

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51856-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51856-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,5 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51856-96:
(7*5)+(6*1)+(5*8)+(4*5)+(3*6)+(2*9)+(1*6)=143
143 % 10 = 3
So 51856-96-3 is a valid CAS Registry Number.

51856-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-pentyl-9-azabicyclo[3.3.1]nonan-3-one

1.2 Other means of identification

Product number -
Other names (1R)-1-pentyl-9-azabicyclo[3.3.1]nonan-3-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:51856-96-3 SDS

51856-96-3Upstream product

51856-96-3Downstream Products

51856-96-3Relevant academic research and scientific papers

Biosynthetic studies on adaline and adalinine, two alkaloids from ladybird beetles (Coleoptera: Coccinellidae)

Laurent, Pascal,Lebrun, Benjamine,Braekman, Jean-Claude,Daloze, Désiré,Pasteels, Jacques M

, p. 3403 - 3412 (2001)

The biosynthesis of the homotropane alkaloid (-)-adaline in the coccinellid beetle Adalia bipunctata has been studied by incorporation experiments with [1-14C] and [2-14C]acetate. A degradation scheme was developed which selectively afforded benzoic acid containing the carbonyl carbon atom of adaline. The labelling pattern thus obtained indicated that the alkaloid is biosynthesized via a polyacetate pathway. Moreover, feeding A. bipunctata adults with (-)-[10,10,11,11,12,12,13,13,14,14,14-2H11] adaline·HCl afforded (-)-[7,7,8,8,9,9,10,10,11,11,11-2H11]adalinine, demonstrating a biogenetic relationship between the two alkaloids. Possible mechanisms for this conversion are discussed. Finally, the synthetic scheme devised to obtain (±)-6-acetonyl-2-pentyl-1-piperideine did not yield the target compound, but afforded instead (±)-adaline in moderate yields. This unexpected result gives support to the hypothesis that this piperideine could be a key intermediate in the biosynthesis of adaline.

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