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diethyl 4-phenylpiperidine-1,4-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14760-44-2

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14760-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14760-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,6 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14760-44:
(7*1)+(6*4)+(5*7)+(4*6)+(3*0)+(2*4)+(1*4)=102
102 % 10 = 2
So 14760-44-2 is a valid CAS Registry Number.

14760-44-2SDS

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 diethyl 4-phenylpiperidine-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names Diethyl-4-phenyl-1,4-piperidindicarboxylat

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:14760-44-2 SDS

14760-44-2Upstream product

14760-44-2Downstream Products

14760-44-2Relevant academic research and scientific papers

Artifacts formed in the metabolic study of pethidine

Stillwell,Lindberg,Hartvig

, p. 71 - 75,72, 74 (2007/10/08)

The condensation of primary and secondary amines with formaldehyde from various sources has caused much confusion in the areas of drug metabolism and biogenic amine metabolism. Nelson et al. identified condensation products of a metabolite of lidocaine and acetaldehyde or formaldehyde present in organic solvents. Biogenic amines have also been found to condense with formaldehyde, enzymatically formed in vivo from 5 methyltetrahydrofolic acid. The presence of N-formylnorpethidine must be due to a condensation between norpethidine and formaldehyde from the organic solvent and/or from biological sources.

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