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24860-78-4

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24860-78-4 Usage

Chemical Class

Piperidines

Physical State

White to off-white solid

Solubility

Soluble in organic solvents

Melting Point

Around 150-155°C

Use

Pharmaceutical intermediate

Potential Applications

Building block for the synthesis of various pharmaceutical drugs

Pharmacological Properties

Potential central nervous system stimulant

Check Digit Verification of cas no

The CAS Registry Mumber 24860-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,6 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24860-78:
(7*2)+(6*4)+(5*8)+(4*6)+(3*0)+(2*7)+(1*8)=124
124 % 10 = 4
So 24860-78-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H27NO2/c24-21(15-10-18-23-16-8-3-9-17-23)22(25,19-11-4-1-5-12-19)20-13-6-2-7-14-20/h1-2,4-7,11-14,25H,3,8-10,15-18H2

24860-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-1,1-diphenyl-5-piperidin-1-ylpentan-2-one

1.2 Other means of identification

Product number -
Other names 2-Pentanone,1,1-diphenyl-1-hydroxy-5-piperidino

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:24860-78-4 SDS

24860-78-4Downstream Products

24860-78-4Relevant articles and documents

Synthesis and antagonistic activity at muscarinic receptor subtypes of some derivatives of diphenidol

Varoli, Lucilla,Angeli, Piero,Buccioni, Michela,Burnelli, Silvia,Cavalli, Andrea,Marucci, Gabriella,Recanatini, Maurizio

, p. 651 - 657 (2007/10/03)

A series of new derivatives, related to diphenidol and to its 2-carbonyl analogue, were designed as antimuscarinic agents. The synthesized compounds were evaluated both as hydrochlorides and as methiodides by functional tests at guinea-pig heart (M2), guinea-pig ileum (M3) and rabbit vas deferens (putative M4). Two derivatives (3a and 5a) showed an M3-selective profile similar to that of the reference compounds, though they resulted less potent.

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