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4-Piperidinol, 1-(trifluoroacetyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93343-02-3

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93343-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93343-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,4 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93343-02:
(7*9)+(6*3)+(5*3)+(4*4)+(3*3)+(2*0)+(1*2)=123
123 % 10 = 3
So 93343-02-3 is a valid CAS Registry Number.

93343-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-1-(4-hydroxypiperidin-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names N-trifluoroacetyl-4-hydroxypiperidine

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:93343-02-3 SDS

93343-02-3Relevant academic research and scientific papers

Nanoscale molecular rods with a new building block for solubility enhancement

Wessig, Pablo,Moellnitz, Kristian

, p. 4452 - 4457 (2008/09/21)

(Chemical Equation Presented) A new building block bearing a [1,3]dioxolo[4,5-f][1,3]benzodioxole core was developed to enhance the solubility of molecular rods by lateral alkyl chains. On incorporation in molecular rods with oligospiroketal structure, the straight geometry is retained, which was concluded from the X-ray crystal structure analysis of one of the rods. The determination of the solubility of a collection of rods bearing this building block revealed that already a butyl group efficiently hinders the aggregation of the rods and consequently causes a considerable enhancement of the solubility. Piperidine rings are located at the ends of the rods, which offer the opportunity for versatile functionalization. Thus, an N,N′-bis(azidoacetyl)-functionalized rod was prepared, which could serve as rigid linkage, initiated by a "Click" reaction.

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