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432-03-1

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432-03-1 Usage

Physical state

Colorless liquid

Odor

Pungent

Uses

a. Reagent in organic synthesis
b. Building block in the production of pharmaceuticals and agrochemicals

Reactivity

Highly reactive

Solvent properties

Strong

Environmental impact

Potent greenhouse gas with high global warming potential

Regulation

Use and production are regulated due to negative environmental impact

Safety precautions

Handle and store with care due to potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 432-03-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 432-03:
(5*4)+(4*3)+(3*2)+(2*0)+(1*3)=41
41 % 10 = 1
So 432-03-1 is a valid CAS Registry Number.

432-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Tris(trifluoromethyl)amine

1.2 Other means of identification

Product number -
Other names Methanamine, 1,1,1-trifluoro-N,N-bis(trifluoromethyl)-

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:432-03-1 SDS

432-03-1Downstream Products

432-03-1Relevant articles and documents

HEXA-, HEPTA- UND OCTAFLUORTRIMETHYLAMIN

Buerger, H.,Niepel, H.,Pawelke, G.,Frohn, H. J.,Sartori, P.

, p. 231 - 238 (1980)

The electrofluorination of N(CH3)3 yields, along with fragmentation and recombination products and N(CF3)3 (I), minor quantities of the hitherto unknown compounds (CF3)2NCF2H (II), CF3N(CF2H)2 (III) and N(CF2H)3 (IV).I-IV have been isolated and characterized by their (1)H, (13)C and (19)F nmr and their EI and CI mass spectra.

Mechanistic studies on the electrochemical fluorination of trialkylamines and tetraalkylammonium salts

Dimitrov,Pfeifer,Jonethal,Ruediger,Seppelt

, p. 143 - 150 (2007/10/03)

The comparative electrochemical fluorination (ECF) of selected trialkylamines and tetraalkylammonium salts was studied in order to obtain experimental data allowing a precise valuation of the ECF mechanism. The results of the investigation favour the ECF mechanism already proposed by Simons, via oxidation of F- .(HF)n to F and nHF, as probably the only relevant electrochemical process at the anode. For the first time some experimental proof has been obtained that a direct electrochemical oxidation of the substrate can be ruled out as a decisive step in ECF.

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