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1258940-00-9

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1258940-00-9 Usage

General Description

(S)-3-phenyl piperidine, also known as (+)-cis-N-Methyl-3-phenylpiperidine, is a chemical compound with the molecular formula C12H17N. It is a chiral intermediate used in the synthesis of various pharmaceutical compounds, including analgesics and antipsychotic medications. The compound is a piperidine derivative with a phenyl group attached to the third carbon atom, and its chiral nature makes it useful in the production of enantiopure drugs. (S)-3-phenyl piperidine is also used as a building block in organic synthesis for the creation of diverse chemical compounds. Due to its versatile applications in the pharmaceutical and chemical industries, (S)-3-phenyl piperidine is a valuable compound for drug development and chemical research.

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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