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Acetic acid, 2,2,2-trifluoro-, 1-ethylpropyl ester, also known as 1-ethylpropyl 2,2,2-trifluoroacetate, is an organic compound with the chemical formula C6H9F3O2. It is a colorless liquid with a molecular weight of 176.13 g/mol. This ester is derived from acetic acid, where the hydroxyl group is replaced by a 1-ethylpropyl group, and the acetic acid molecule contains three fluorine atoms. It is synthesized by reacting 2,2,2-trifluoroacetic acid with 1-ethylpropyl alcohol in the presence of a catalyst. Acetic acid, 2,2,2-trifluoro-, 1-ethylpropyl ester is used as a reagent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals, due to its unique reactivity and properties. It is also known for its potential applications in the production of fluorinated compounds, which have various industrial and commercial uses.

7556-81-2

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7556-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7556-81-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7556-81:
(6*7)+(5*5)+(4*5)+(3*6)+(2*8)+(1*1)=122
122 % 10 = 2
So 7556-81-2 is a valid CAS Registry Number.

7556-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name pentan-3-yl 2,2,2-trifluoroacetate

1.2 Other means of identification

Product number -
Other names 3-pentyl trifluoroacetate

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:7556-81-2 SDS

7556-81-2Downstream Products

7556-81-2Relevant academic research and scientific papers

Kinetics and mechanism of nucleophilic displacements with heterocycles as leaving groups. Part 23. Studies at the borderlines between reactions proceeding (i) via free carbocations, (ii) via rate-determining formation of ion-molecule pairs, and (iii) via rate-determining nucleophilic ...

Katritzky, Alan R.,Brycki, Bogumil

, p. 1161 - 1169 (2007/10/02)

Evidenece is presented to demonstrate that at the borderline between first order reaction via the formation of free carbocations, both mechanism proceed independently, without merging.Similarly at the borderline between first-order (rate determining formation) and second-order (rate-determining nucleophilic attack) rections of intimate ion-molecule pairs, both reactions again proceed independently.

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