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3-(Cyclopentylmethyl)pyridine is an organic compound characterized by a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a cyclopentylmethyl group attached to the third carbon of the pyridine. 3-(cyclopentylmethyl)pyridine is a colorless liquid with a molecular formula of C12H17N and a molecular weight of 175.27 g/mol. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound is insoluble in water but soluble in organic solvents such as ethanol, acetone, and dichloromethane. It is also known for its potential applications in the development of new materials and as a ligand in coordination chemistry.

6311-85-9

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6311-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6311-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6311-85:
(6*6)+(5*3)+(4*1)+(3*1)+(2*8)+(1*5)=79
79 % 10 = 9
So 6311-85-9 is a valid CAS Registry Number.

6311-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(cyclopentylmethyl)pyridine

1.2 Other means of identification

Product number -
Other names 3-cyclopentylmethyl-pyridine

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

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More Details:6311-85-9 SDS

6311-85-9Downstream Products

6311-85-9Relevant academic research and scientific papers

Tandem intramolecular carbolithiation-lithium/zinc transmetallation and applications to carbon-carbon bond-forming reactions

Yus, Miguel,Ortiz, Rosa

, p. 3833 - 3841 (2007/10/03)

Lithium/zinc transmetallation with the cyclic organolithium intermediate 3 (prepared by intramolecular carbolithiation of the initially formed organolithium 2) gives the corresponding organozinc intermediate 5. Copper- or palladium-promoted SN2

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