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39512-49-7

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39512-49-7 Usage

Uses

4-(4-Chlorophenyl)-4-hydroxypiperidine can be used as potential fluorescent sigma receptor probes.

Check Digit Verification of cas no

The CAS Registry Mumber 39512-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39512-49:
(7*3)+(6*9)+(5*5)+(4*1)+(3*2)+(2*4)+(1*9)=127
127 % 10 = 7
So 39512-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H14ClNO/c12-10-3-1-9(2-4-10)11(14)5-7-13-8-6-11/h1-4,13-14H,5-8H2/p+1

39512-49-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A12137)  4-(4-Chlorophenyl)-4-hydroxypiperidine, 97%   

  • 39512-49-7

  • 1g

  • 315.0CNY

  • Detail
  • Alfa Aesar

  • (A12137)  4-(4-Chlorophenyl)-4-hydroxypiperidine, 97%   

  • 39512-49-7

  • 5g

  • 980.0CNY

  • Detail
  • Alfa Aesar

  • (A12137)  4-(4-Chlorophenyl)-4-hydroxypiperidine, 97%   

  • 39512-49-7

  • 25g

  • 3778.0CNY

  • Detail
  • Aldrich

  • (C66056)  4-(4-Chlorophenyl)-4-hydroxypiperidine  99%

  • 39512-49-7

  • C66056-5G

  • 1,005.03CNY

  • Detail

39512-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-Chlorophenyl)piperidin-4-ol

1.2 Other means of identification

Product number -
Other names 4-Piperidinol, 4-(4-chlorophenyl)-

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:39512-49-7 SDS

39512-49-7Relevant articles and documents

Preparation method of flupiperidinol

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Paragraph 0089; 0093-0094; 0098; 0102-0103, (2021/03/24)

The invention belongs to the technical field of medicine preparation, and particularly relates to a preparation method of flupiperidinol. The preparation method of the fluoropiperidinol, provided by the invention, comprises the following steps of providing 4-(4-chlorphenyl)-4-piperidinol of which the purity is 99% or above, providing 4-chloro-1-(4-fluorophenyl)butan-1-one of which the purity is more than 99%, mixing the 4-(4-chlorphenyl)-4-piperidinol, 4-chloro-1-(4-fluorophenyl)butan-1-one, an alkaline substance and a catalyst, and carrying out a first substitution reaction to obtain a crudeproduct, and mixing the crude product with an organic solvent, and sequentially carrying out reflux and crystallization to obtain the flupiperidinol. The flupiperidinol prepared according to the preparation method provided by the invention has relatively high yield and purity.

Remote C(sp3)-H Oxygenation of Protonated Aliphatic Amines with Potassium Persulfate

Lee, Melissa,Sanford, Melanie S.

supporting information, p. 572 - 575 (2017/02/10)

This letter describes the development of a method for selective remote C(sp3)-H oxygenation of protonated aliphatic amines using aqueous potassium persulfate. Protonation serves to deactivate the proximal C(sp3)-H bonds of the amine substrates and also renders the amines soluble in the aqueous medium. These reactions proceed under relatively mild conditions (within 2 h at 80 °C with amine as limiting reagent) and do not require a transition metal catalyst. This method is applicable to a variety of types of C(sp3)-H bonds, including 3°, 2°, and benzylic C-H sites in primary, secondary, and tertiary amine substrates.

METALLO-BETA-LACTAMASE INHIBITORS

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, (2015/08/06)

The present invention relates to compounds of formula (I) that are metallo-β-lactamase inhibitors, the synthesis of such compounds, and the use of such compounds for use with β-lactam antibiotics for overcoming resistance.

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