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(3S,4R)-3-METHYL-4-N-PHENYLAMINO-PIPERIDINE is a piperidine derivative with the molecular formula C13H20N2. It features a methyl group at the third position and a phenylamino group at the fourth position. (3S,4R)-3-METHYL-4-N-PHENYLAMINO-PIPERIDINE's stereochemistry, with the (3S,4R) configuration, is crucial for its pharmacological properties and potential interactions with biological targets. Given the presence of both a piperidine and an amino group, which are common structural motifs in many drugs, (3S,4R)-3-METHYL-4-N-PHENYLAMINO-PIPERIDINE has potential pharmaceutical applications. Further research is needed to fully understand its physiological effects and potential applications.

53757-51-0

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53757-51-0 Usage

Uses

Used in Pharmaceutical Industry:
(3S,4R)-3-METHYL-4-N-PHENYLAMINO-PIPERIDINE is used as a chemical compound with potential pharmaceutical applications due to its unique structure and stereochemistry. Its presence of a piperidine and an amino group makes it a promising candidate for the development of new drugs. Further research is required to explore its specific applications and therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 53757-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,5 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53757-51:
(7*5)+(6*3)+(5*7)+(4*5)+(3*7)+(2*5)+(1*1)=140
140 % 10 = 0
So 53757-51-0 is a valid CAS Registry Number.

53757-51-0SDS

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 (3S,4R)-3-METHYL-4-N-PHENYLAMINO-PIPERIDINE

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

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More Details:53757-51-0 SDS

53757-51-0Relevant academic research and scientific papers

Enantiomers of Diastereomeric cis-N--N-phenylpropanamides: Synthesis, X-ray Analysis, and Biological Activities

Brine, George A.,Stark, Peter A.,Liu, Young,Carrol, F. Ivy,Singh, P.,et al.

, p. 1547 - 1557 (2007/10/02)

(+/-)-cis-N--N-phenylpropanamide (1) is a mixture of four stereoisomers , which together constitute two diastereoisomeric pairs of optical i

Stereoisomers of N-[1-(2-hydroxy-2-phenylethyl)-3-methyl-4-piperidyl]-N- phenylpropanamide: Synthesis, stereochemistry, analgesic activity, and opioid receptor binding characteristics

Wang,Zhu,Jin,Chen,Chen,Ji,Chi

, p. 3652 - 3659 (2007/10/03)

N-[1-(2-Hydroxy-2-phenylethyl)-3-methyl-4-piperidyl]-N-phenylpropanamide (ohmefentanyl, 1) is an extremely potent analgesic agent with high affinity and selectivity for opioid μ receptors. There are three chiral carbons in 1, so eight optically active iso

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