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1,3,7,7-Tetramethylnorbornan-2-one is a cyclic ketone with the molecular formula C11H18O. It is a colorless to pale yellow liquid with a strong, pungent odor. 1,3,7,7-Tetramethylnorbornan-2-one is a derivative of norbornanone, a bicyclic ketone, and is characterized by the presence of four methyl groups attached to the carbon atoms at positions 1, 3, 7, and 7. It is synthesized through various chemical reactions, such as the Diels-Alder reaction, and is used as an intermediate in the production of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential applications, 1,3,7,7-Tetramethylnorbornan-2-one has been the subject of research in organic chemistry and synthetic chemistry.

5811-48-3

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5811-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5811-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5811-48:
(6*5)+(5*8)+(4*1)+(3*1)+(2*4)+(1*8)=93
93 % 10 = 3
So 5811-48-3 is a valid CAS Registry Number.

5811-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylcamphor

1.2 Other means of identification

Product number -
Other names 1,3,7,7-Tetramethyl-norbornan-2-on

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:5811-48-3 SDS

5811-48-3Relevant academic research and scientific papers

NICOTINIC RECEPTOR NON-COMPETITIVE ANTAGONISTS

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Page/Page column 40-41, (2014/01/17)

The present invention relates to compounds that modulate nicotinic receptors as non-competitive antagonists, methods for their synthesis, methods for their use, and their pharmaceutical compositions.

Reactions of halonorbornane and oxo-substituted derivatives with different anions by the electron transfer mechanism; Redox catalysis in stabilized radicals

Uranga, Jorge G.,Santiago, Ana N.

scheme or table, p. 2006 - 2012 (2011/01/10)

Reactions of 2-bromo-, 2-chloronorbornane, 3-chloronorbornan-2-one and 3-bromocamphor with Me3Sn-, Ph2P- or PhS- ions were studied by an SRN1 mechanism in liquid ammonia or DMSO. The results show that substrates having a carbonyl group facilitate electron transfer reactions, which are impeded in the absence of such a group. However, when the free radical formed is stabilized by conjugation, the coupling reaction decreases, causing a concomitant increase in the reduction product. Theoretical studies explain the observed reactivity on the basis of a mechanism involving reductive cleavage as a function of the π-σ interactions.

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