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3512-18-3

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3512-18-3 Usage

Chemical Properties

Colorless liquid

Uses

2,3,6-Trifluoropyridine is used as an intermediate in organic syntheses and in pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 3512-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3512-18:
(6*3)+(5*5)+(4*1)+(3*2)+(2*1)+(1*8)=63
63 % 10 = 3
So 3512-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H2F3N/c6-3-1-2-4(7)9-5(3)8/h1-2H

3512-18-3 Well-known Company Product Price

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  • (Code)Product description
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  • Price
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  • Alfa Aesar

  • (L19540)  2,3,6-Trifluoropyridine, 97%   

  • 3512-18-3

  • 1g

  • 380.0CNY

  • Detail
  • Alfa Aesar

  • (L19540)  2,3,6-Trifluoropyridine, 97%   

  • 3512-18-3

  • 5g

  • 1265.0CNY

  • Detail

3512-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6-Trifluoropyridine

1.2 Other means of identification

Product number -
Other names 2,3,4-TRICB UNLABELED

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:3512-18-3 SDS

3512-18-3Relevant articles and documents

Rhodium catalyzed, carbon-hydrogen bond directed hydrodefluorination of fluoroarenes

Ekkert, Olga,Strudley, Sebastian D. A.,Rozenfeld, Alisa,White, Andrew J. P.,Crimmin, Mark R.

supporting information, p. 7027 - 7030 (2015/05/19)

[CpRhCl(μ-Cl)]2 is reported as a highly efficient and selective precatalyst for the hydrodefluorination of perfluoroarenes using a hydrocarbon-soluble aluminum dihydride as the terminal reductant. Reactions are directed to cleave a C-F bond adjacent to an existing C-H bond with high regioselectivity (98.5-99%). A heterobimetallic complex containing an extremely rare Al-H-Rh functional group has been isolated and shown to be catalytically competent.

Heterocyclic derivatives

-

, (2008/06/13)

The invention relates to heterocyclic derivatives of the formula I wherein R1, A1, Z1, n, A2, Z2, Q1, Q2, Q3 and L have the meaning given in claim 1 and to their use as components of liquid crystalline media for electro-optical displays.

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