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Piperidine, 1-(cyclohexylidenemethyl)-, also known as 1-(Cyclohexylmethyl)piperidine, is an organic compound with the chemical formula C12H23N. It is a derivative of piperidine, a heterocyclic amine, with a cyclohexylmethyl group attached to the nitrogen atom. Piperidine, 1-(cyclohexylidenemethyl)- is a colorless liquid with a density of 0.92 g/cm3 and a boiling point of 250-252°C. It is soluble in organic solvents and has a mild amine-like odor. 1-(Cyclohexylmethyl)piperidine is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a chiral auxiliary in asymmetric synthesis and as a ligand in catalysis. Due to its potential applications in the chemical industry, it is essential to handle Piperidine, 1-(cyclohexylidenemethyl)- with care, as it may have toxic effects on human health and the environment.

6604-81-5

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6604-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6604-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6604-81:
(6*6)+(5*6)+(4*0)+(3*4)+(2*8)+(1*1)=95
95 % 10 = 5
So 6604-81-5 is a valid CAS Registry Number.

6604-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexylidenemethyl-piperidine

1.2 Other means of identification

Product number -
Other names -

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:6604-81-5 SDS

6604-81-5Relevant academic research and scientific papers

A mild oxidation of aldehydes to α,β-unsaturated aldehydes

Williams, David R.,Nishitani, Kiyoshi

, p. 4417 - 4420 (2007/10/02)

Phenylselenenyl chloride reacts with enamines at -110° C to give α-phenylselenoaldehydes, and oxidative elimination yields α,β-unsaturated aldehydes.

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