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6856-31-1

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6856-31-1 Usage

Chemical Properties

White to Off-White Crystalline Powder

Uses

Pridinol Methanesulfonate Salt can be used as an antiparkinsonian agent and as an anticholinergic.

Check Digit Verification of cas no

The CAS Registry Mumber 6856-31-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6856-31:
(6*6)+(5*8)+(4*5)+(3*6)+(2*3)+(1*1)=121
121 % 10 = 1
So 6856-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H25NO.CH4O3S/c22-17-14-20(18-10-4-1-5-11-18,19-12-6-2-7-13-19)21-15-8-3-9-16-21;1-5(2,3)4/h1-2,4-7,10-13,22H,3,8-9,14-17H2;1H3,(H,2,3,4)

6856-31-1 Well-known Company Product Price

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  • Sigma-Aldrich

  • (P4419)  Pridinolmethanesulfonatesalt  analytical standard

  • 6856-31-1

  • P4419-5G

  • 506.61CNY

  • Detail
  • Sigma-Aldrich

  • (P4419)  Pridinolmethanesulfonatesalt  analytical standard

  • 6856-31-1

  • P4419-25G

  • 1,264.77CNY

  • Detail

6856-31-1SDS

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 Pridinol Methanesulfonate Salt

1.2 Other means of identification

Product number -
Other names 1,1-diphenyl-3-piperidin-1-ylpropan-1-ol,methanesulfonic acid

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:6856-31-1 SDS

6856-31-1Downstream Products

6856-31-1Relevant articles and documents

A methanesulfonic acid pu vertical preparation method

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Paragraph 0021; 0022; 0023; 0024, (2017/06/02)

The invention discloses a preparation method of pridinol mesylate. The preparation method comprises the following steps: carrying out reaction on methyl acrylate and piperidine to obtain methyl 3-(1-piperidyl) propionate, carrying out reaction on methyl 3-(1-piperidyl) propionate and phenyl magnesium bromide (as a Grignard reagent) to obtain pridinol, and forming a salt by pridinol and methanesulfonic acid in a solvent such as an ether solvent to obtain pridinol mesylate as a final product. The process route is simple in synthetic steps, is short in reaction route, is high in yield and is economical and practical.

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