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2-methylbicyclo[3.2.1]octan-2-ol is a cyclic organic compound with the molecular formula C10H18O. It features a bicyclo[3.2.1]octane ring structure, which consists of three fused rings with a total of eight carbon atoms, and a methyl group attached to the second carbon atom. The hydroxyl group (-OH) is present at the second carbon atom as well, making it a secondary alcohol. 2-methylbicyclo[3.2.1]octan-2-ol is known for its unique structure and potential applications in the synthesis of various organic compounds, particularly in the pharmaceutical and chemical industries. It is also recognized for its distinct chemical properties, such as its ability to form hydrogen bonds due to the presence of the hydroxyl group, which can influence its reactivity and solubility in different solvents.

5019-84-1

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5019-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5019-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,1 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5019-84:
(6*5)+(5*0)+(4*1)+(3*9)+(2*8)+(1*4)=81
81 % 10 = 1
So 5019-84-1 is a valid CAS Registry Number.

5019-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylbicyclo[3.2.1]octan-4-ol

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-2-methylbicyclo[3.2.1]octan

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 -
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More Details:5019-84-1 SDS

5019-84-1Downstream Products

5019-84-1Relevant academic research and scientific papers

On the Stereochemistry of Grignard Addition to Bicyclononan-2-one. Preferential Axial Attack on a Cyclohexanone System by a Bulky Nucleophile

Guerriero, Antonio,Pietra, Francesco,Cavazza, Marino,Cima, Francesco Del

, p. 979 - 982 (2007/10/02)

Bicyclononan-2-one (1) reacts with methylmagnesium iodide to give, in a high overall yield, a 19:1 mixture of exo-2-methylbicyclononan-2-ol (2) and the endo-epimer (3), respectively.The high propensity of compound (1) for axial attack by a bulky reagent, such as a Grignard reagent, is atypical of bridged cyclohexanones.Possibly, flattening of the bicyclononan-2-one skeleton favours axial attack.Results of the oxymercuriation-demercuriation of related olefins is in accordance with this view.

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