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Propionic acid (3S)-1,3α-dimethyl-4-phenylpiperidine-4β-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25123-06-2

25123-06-2 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

25123-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25123-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25123-06:
(7*2)+(6*5)+(5*1)+(4*2)+(3*3)+(2*0)+(1*6)=72
72 % 10 = 2
So 25123-06-2 is a valid CAS Registry Number.

25123-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-β-prodine

1.2 Other means of identification

Product number -
Other names Propionic acid (3S,4S)-1,3-dimethyl-4-phenyl-piperidin-4-yl 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:25123-06-2 SDS

25123-06-2Relevant academic research and scientific papers

The morphine-like and nonmorphine-like conformers of prodine opioids

Khanolkar, Atmaram D.,Yin, Dali,Makriyannis, Alexandros,Brooks, Andrew I.,Pasternak, Gavril W.,Froimowitz, Mark

, p. 11 - 21 (2007/10/03)

The compounds α-, and β-prodine and their meta hydroxylated analogs were synthesized, resolved, and screened for affinity at opioid receptor subtypes. The compounds primarily have affinity for μ-receptors. The μ-receptor affinities of the nonmorphine-like (+)-enantiomers, which have the greater antinociceptive activity, are reduced by the presence of a meta hydroxyl while the affinities for all opioid receptor subtypes of the morphine-like, but less active, (-)-enantiomers are enhanced or unchanged. Both enantiomers of meta-hydroxylated β-prodine had antagonist activity in the guinea pig ileum assay.