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1619-92-7

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1619-92-7 Usage

General Description

1,1,1,3,3,3-Hexafluoroisopropylamine, also known as HFI, is a fluorinated amine compound with the chemical formula C3H2F6N. It is a highly volatile and flammable liquid with a strong ammonia-like odor. HFI is primarily used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used as a solvent and as a reagent in organic reactions. HFI is considered to be a hazardous substance and should be handled with caution due to its potential for toxicity and environmental harm.

Check Digit Verification of cas no

The CAS Registry Mumber 1619-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1619-92:
(6*1)+(5*6)+(4*1)+(3*9)+(2*9)+(1*2)=87
87 % 10 = 7
So 1619-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H3F6N/c4-2(5,6)1(10)3(7,8)9/h1H,10H2

1619-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,3,3,3-hexafluoropropan-2-amine

1.2 Other means of identification

Product number -
Other names 2-hydrohexafluoro-2-propanamine

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:1619-92-7 SDS

1619-92-7Relevant articles and documents

REACTION OF INTERNAL PERFLUORINATED α-OXIDES WITH AMMONIA

Saloutina, L. V.,Zapevalov, A. Ya.,Kodess, M. I.,Kolenko, I. P.

, p. 628 - 634 (2007/10/02)

The action of ammonia leads to nucleophilic opening of the epoxide ring in internal perfluorinated α oxides with the formation of aminoiminoperfluoroalkanols and their dissociation products.In unsymmetrical disubstituted 2,3-epoxyperfluoroalkanes attack by ammonia at the carbon atoms of the epoxide ring is not regioselective, whereas in the trisubstituted compounds regiospecific reaction with ammonia occurs.The stability of the internal perfluorinated α-oxides to the action of ammonia is increased with increase in the size of the fluoroalkyl substituents.

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