Welcome to LookChem.com Sign In|Join Free

CAS

  • or

83863-40-5

Post Buying Request

83863-40-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

83863-40-5 Usage

Description

4-phenyl-1-(p-tolylsulphonyl)piperidin-4-ol is a chemical compound with a molecular formula C21H23NO3S. It is a piperidine derivative that contains a phenyl group and a p-tolylsulphonyl group attached to a piperidine ring. 4-phenyl-1-(p-tolylsulphonyl)piperidin-4-ol has potential pharmaceutical applications due to its structural similarity to other piperidine-based drugs. The presence of the hydroxyl group in the piperidine ring suggests that it may have some physiological activity, possibly as a potential drug candidate or as a chemical intermediate in the synthesis of other compounds. However, further research and testing are needed to fully understand the properties and potential uses of this chemical.

Uses

Used in Pharmaceutical Industry:
4-phenyl-1-(p-tolylsulphonyl)piperidin-4-ol is used as a potential drug candidate for various therapeutic applications due to its structural similarity to other piperidine-based drugs. Its unique chemical structure, including the phenyl and p-tolylsulphonyl groups, may contribute to its potential pharmacological properties and therapeutic effects.
Used as a Chemical Intermediate:
4-phenyl-1-(p-tolylsulphonyl)piperidin-4-ol can be used as a chemical intermediate in the synthesis of other compounds, particularly in the development of new pharmaceuticals. Its unique structure and functional groups may be utilized in the design and synthesis of novel drug molecules with improved therapeutic properties.
Note: The specific applications and reasons for using 4-phenyl-1-(p-tolylsulphonyl)piperidin-4-ol in different industries are not provided in the materials. The uses mentioned above are based on the general potential of this compound as a pharmaceutical candidate and chemical intermediate. Further research and testing are required to determine its exact applications and benefits in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 83863-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,6 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83863-40:
(7*8)+(6*3)+(5*8)+(4*6)+(3*3)+(2*4)+(1*0)=155
155 % 10 = 5
So 83863-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H21NO3S/c1-15-7-9-17(10-8-15)23(21,22)19-13-11-18(20,12-14-19)16-5-3-2-4-6-16/h2-10,20H,11-14H2,1H3

83863-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenyl)sulfonyl-4-phenylpiperidin-4-ol

1.2 Other means of identification

Product number -
Other names EINECS 281-102-4

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:83863-40-5 SDS

83863-40-5Relevant articles and documents

Synthesis of cis-3,4-diarylpiperidines and cis-3,4-diaryltetrahydropyrans

Chang, Meng-Yang,Lin, Chun-Yu,Hung, Ching-Yi

, p. 3312 - 3320 (2007/10/03)

Substituted cis-3,4-diarylpiperidines and cis-3,4-diaryltetrahydropyrans are synthesized in modest overall yields starting from 4-aryl-1,2,5,6-tetrahydropyridines and 4-aryl-1,2,5,6-tetrahydropyrans via the following sequence: (1) pinacol-type ring contraction having the?combination of m-chloroperoxybenzoic acid and boron trifluoride etherate, (2) Grignard addition with arylmagnesium bromide reagents and followed by boron trifluoride etherate-mediated intramolecular ring-expanded rearrangement, and (3) hydrogenation with hydrogen on 10% palladium-activated carbon. A facile synthesis of 3,4-diarylpyridines was also described by base-induced aromatization.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 83863-40-5