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65195-20-2

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65195-20-2 Usage

Uses

2-(1-Piperidinyl)phenol is used as primary and secondary intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 65195-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,9 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65195-20:
(7*6)+(6*5)+(5*1)+(4*9)+(3*5)+(2*2)+(1*0)=132
132 % 10 = 2
So 65195-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO/c13-11-7-3-2-6-10(11)12-8-4-1-5-9-12/h2-3,6-7,13H,1,4-5,8-9H2

65195-20-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L07630)  2-(1-Piperidinyl)phenol, 98%   

  • 65195-20-2

  • 1g

  • 574.0CNY

  • Detail
  • Alfa Aesar

  • (L07630)  2-(1-Piperidinyl)phenol, 98%   

  • 65195-20-2

  • 5g

  • 2215.0CNY

  • Detail

65195-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-piperidin-1-ylphenol

1.2 Other means of identification

Product number -
Other names N-<2-Hydroxy-phenyl>-piperidin

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:65195-20-2 SDS

65195-20-2Relevant articles and documents

Iron-Catalyzed Direct Alkylamination of Phenols with O-Benzoyl-N-alkylhydroxylamines under Mild Conditions

Jia, Lei,Gao, Sen,Xie, Junyao,Luo, Meiming

, p. 3840 - 3846 (2016/12/16)

A novel iron-catalyzed direct alkylamination reaction of phenols has been achieved with O-benzoyl-N-alkylhydroxylamines as aminating agents. This protocol provides a facile access to N-alkyl-substituted aminophenols though a radical reaction from phenols. The catalytic direct alkylamination operates at room temperature without the need of any ligands and additives to afford the desired products with excellent regioselectivity and functional group tolerance. (Figure presented.).

Selective Preparations; 34. A Convenient Preparation of 2-Piperidinophenols

Tashiro, Masashi,Fukata, Gouki,Itoh, Takashi

, p. 489 - 490 (2007/10/02)

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