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145678-87-1

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145678-87-1 Usage

Uses

(-)-(3S,4S)-3,4-Dimethyl-4-(3-hydroxyphenyl)piperidine is a key intermediate used in the preparation of the opioid drug Alvimopan.

Check Digit Verification of cas no

The CAS Registry Mumber 145678-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,7 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 145678-87:
(8*1)+(7*4)+(6*5)+(5*6)+(4*7)+(3*8)+(2*8)+(1*7)=171
171 % 10 = 1
So 145678-87-1 is a valid CAS Registry Number.

145678-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(3R,4S)-3,4-dimethylpiperidin-4-yl]phenol

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:145678-87-1 SDS

145678-87-1Relevant articles and documents

Synthesis and characterization of all possible diastereoisomers of alvimopan

Reddy, Beeravalli Ramalinga,Dubey, Manoj Kumar,Ramana Reddy, Ch. Venkata,Bandichhor, Rakeshwar

, p. 963 - 972 (2018/05/28)

Isolation of all possible diastereomers of alvimopan 1 was found to be challenging. In order to perform cut off studies during analytical method development, it was mandatory to synthesize and characterize all the diastereomeric impurities. Here in, our efforts toward the synthesis and isolation of alvimopan (1) diastereomers are discussed.

1,3,4-Trisubstituted-4-arylpiperidines and their preparation

-

, (2008/06/13)

Novel 1,3,4-trisubstituted-4-arylpiperidines are prepared by alkylating a 2,3-disubstituted-3-arylpyrroline to afford a 1,2,3-trisubstituted-3-aryl-1-pyrrolinium salt, reacting the salt with diazomethane to provide a 1,2,3-trisubstituted-3-aryl-1,2-methyl

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