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(S)-3-PHENYL PIPERIDINE, also known as (+)-cis-N-Methyl-3-phenylpiperidine, is a chiral intermediate with the molecular formula C12H17N. It is a piperidine derivative featuring a phenyl group attached to the third carbon atom. (S)-3-PHENYL PIPERIDINE's chiral nature and versatile applications in the pharmaceutical and chemical industries make it a valuable compound for drug development and chemical research.

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  • 1258940-00-9 Structure
  • Basic information

    1. Product Name: (S)-3-PHENYL PIPERIDINE
    2. Synonyms: (S)-3-PHENYL PIPERIDINE;(S)-3-Phenyl-piperidine hydrochloride
    3. CAS NO:1258940-00-9
    4. Molecular Formula: C11H15N*ClH
    5. Molecular Weight: 161.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1258940-00-9.mol
  • Chemical Properties

    1. Melting Point: 178.2-178.4 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-3-PHENYL PIPERIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-PHENYL PIPERIDINE(1258940-00-9)
    11. EPA Substance Registry System: (S)-3-PHENYL PIPERIDINE(1258940-00-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1258940-00-9(Hazardous Substances Data)

1258940-00-9 Usage

Uses

Used in Pharmaceutical Industry:
(S)-3-PHENYL PIPERIDINE is used as a chiral intermediate for the synthesis of various pharmaceutical compounds, including analgesics and antipsychotic medications. Its chiral nature allows for the production of enantiopure drugs, which can have different therapeutic effects and reduce potential side effects.
Used in Organic Synthesis:
(S)-3-PHENYL PIPERIDINE is used as a building block in organic synthesis for the creation of diverse chemical compounds. Its versatile structure enables the development of new molecules with potential applications in various fields, such as materials science, agrochemicals, and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1258940-00-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,9,4 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1258940-00:
(9*1)+(8*2)+(7*5)+(6*8)+(5*9)+(4*4)+(3*0)+(2*0)+(1*0)=169
169 % 10 = 9
So 1258940-00-9 is a valid CAS Registry Number.

1258940-00-9SDS

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 (S)-3-phenylpiperidine hydrochloride

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:1258940-00-9 SDS

1258940-00-9Downstream Products

1258940-00-9Relevant articles and documents

Asymmetric synthesis of chiral N-sulfinyl 3-alkyl- and 3-arylpiperidines by α-alkylation of N-sulfinyl imidates with 1-chloro-3-iodopropane

Colpaert, Filip,Mangelinckx, Sven,De Kimpe, Norbert

, p. 234 - 244 (2011/03/19)

α-Alkylation of N-sulfinyl imidates with 1-chloro-3-iodopropane successfully led to 2-substituted N-tert-butanesulfinyl-5-chloropentanimidates in acceptable diastereomeric ratios (dr 67/33 to 72/28) and good yields (74-86%). Subsequent reduction with NaBH4 led to the corresponding 2-substituted N-tert-butanesulfinyl-5-chloropentylamines, which could be cyclized to a range of new chiral 3-substituted N-tert-butanesulfinylpiperidines using NaH in DMSO. Finally, the N-tert-butanesulfinylpiperidines could be efficiently deprotected to enantiomerically pure 3-alkyl- and 3-arylpiperidine hydrochlorides.

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