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Pyridine, 1,2,3,6-tetrahydro-4-(3-methoxyphenyl)-1,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123004-53-5

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123004-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123004-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,0 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123004-53:
(8*1)+(7*2)+(6*3)+(5*0)+(4*0)+(3*4)+(2*5)+(1*3)=65
65 % 10 = 5
So 123004-53-5 is a valid CAS Registry Number.

123004-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-methoxyphenyl)-1,5-dimethyl-3,6-dihydro-2H-pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,1,2,3,6-tetrahydro-4-(3-methoxyphenyl)-1,5-dimethyl

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:123004-53-5 SDS

123004-53-5Relevant academic research and scientific papers

A stereoselective synthetic approach to N-alkyl-4β-methyl-5- phenylmorphans

Thomas, James B.,Gigstad, Kenneth M.,Fix, Scott E.,Burgess, Jason P.,Cooper, Julie B.,Mascarella, S. Wayne,Cantrell, Buddy E.,Zimmerman, Dennis M.,Carroll, F. Ivy

, p. 403 - 406 (2007/10/03)

A convergent, highly stereoselective synthetic approach to N-alkyl-4β- methyl-5-phenylmorphans has been developed utilizing alkylation of the metalloenamine of N-alkyl-1,2,3,6-tetrahydro-4-phenylpyridines with 2- (chloromethyl)-3,5-dioxahex-1-ene (Okahara's reagent) followed by Clemmensen reduction.

Synthesis of Picenadol via Metalloenamine Alkylation Methodology

Barnett, Charles J.,Copley-Merriman, Catherine R.,Maki, James

, p. 4795 - 4800 (2007/10/02)

A convenient synthesis of the novel phenylpiperidine analgesic agent picenadol, (+/-)-1, via tetrahydropyridine 2 is described.Tetrahydropyridine 7, prepared from 6 via metalation (n-butyllithium) and alkylation with 1-bromopropane, could not be directly

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