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Bicyclo[5.2.1]decane is a cyclic hydrocarbon compound with the molecular formula C10H16. It features a bicyclic structure, consisting of two fused cyclohexane and cyclopentane rings. The compound is known for its unique shape, which includes five carbon atoms in one ring and two carbon atoms in the other, connected by a bridge of three carbon atoms. Bicyclo[5.2.1]decane is an important structural motif in organic chemistry, often found in various natural products and pharmaceuticals. It is also used as a building block for the synthesis of more complex molecules and has applications in the development of new materials and compounds.

284-24-2

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284-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 284-24-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 284-24:
(5*2)+(4*8)+(3*4)+(2*2)+(1*4)=62
62 % 10 = 2
So 284-24-2 is a valid CAS Registry Number.

284-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[5.2.1]decane

1.2 Other means of identification

Product number -
Other names Bicyclo [5,2,1] decan

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:284-24-2 SDS

284-24-2Relevant academic research and scientific papers

A NEW APPROACH TO THE BICYCLO ( 5.2.1 ) DECANE SYSTEM.

Klimko, Yu. E.,Isaev, S. D.,Yurchenko, A. G.

, p. 3259 - 3260 (2007/10/02)

A simple route to the bicyclo ( 5.2.1 ) decane system by oxidation of trimethylenenorbornane is demonstrated.

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