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651053-80-4

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651053-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651053-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,0,5 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 651053-80:
(8*6)+(7*5)+(6*1)+(5*0)+(4*5)+(3*3)+(2*8)+(1*0)=134
134 % 10 = 4
So 651053-80-4 is a valid CAS Registry Number.

651053-80-4SDS

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 phenyl 4-ethylpiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Piperidinecarboxylic acid,4-ethyl-,phenyl ester

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:651053-80-4 SDS

651053-80-4Downstream Products

651053-80-4Relevant articles and documents

Efficient Solution-Phase Parallel Synthesis of 4-Substituted N-Protected Piperidines

Wang, Xiaoyang,Kauppi, Anna M.,Olsson, Roger,Almqvist, Fredrik

, p. 4586 - 4592 (2007/10/03)

Practical conditions for the synthesis of 4-substituted N-protected piperidines through CuCN·2LiBr-catalyzed organozinc additions to 1-acylpyridinium salts and subsequent hydrogen-transfer hydrogenation have been established. The reaction sequence is performed at room temperature and provides 4-substituted N-protected piperidines in excellent overall yields without the isolation of intermediate dihydropyridines, In those cases in which the organozinc addition results in mixtures of 2- and 4-substituted dihydropyridines, the 2-substituted isomers are efficiently scavenged with maleic anhydride and subsequently removed by a mild extractive workup with NaHCO3 (sat.). The N-acyl group can conveniently be exchanged from N-phenoxycarbonyl to N-tBoc, thus allowing orthogonal deprotection strategies. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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