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Heptyl trifluoroacetate, also known as 1-heptyl trifluoroacetate or heptyl trifluoroacetate, is an organic compound with the chemical formula C9H15F3O2. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 216.21 g/mol. heptyl trifluoroacetate is derived from heptyl alcohol and trifluoroacetic acid, and it is commonly used as a solvent, a reagent in organic synthesis, and a component in the production of pharmaceuticals and agrochemicals. Due to its unique properties, such as its low boiling point and high reactivity, heptyl trifluoroacetate plays a significant role in various chemical processes and applications.

2710-89-6

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2710-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2710-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2710-89:
(6*2)+(5*7)+(4*1)+(3*0)+(2*8)+(1*9)=76
76 % 10 = 6
So 2710-89-6 is a valid CAS Registry Number.

2710-89-6SDS

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 heptyl 2,2,2-trifluoroacetate

1.2 Other means of identification

Product number -
Other names Acetic acid,trifluoro,heptyl ester

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 -
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More Details:2710-89-6 SDS

2710-89-6Downstream Products

2710-89-6Relevant academic research and scientific papers

Oxidative Displacement of Halogen from Alkyl Halides by Phenyliodine(III) Dicarboxylates

Gallos, John,Varvoglis, Anastasios

, p. 1999 - 2002 (2007/10/02)

The reaction of alkyl iodides with aryliodine(III) dicarboxylates affords as the main product the ester derived through substitution of iodine by an acyloxy group; in some cases α-iodoalkyl esters are also formed along with other minor products.Certain reactive bromides and chlorides react along similar lines.The mechanism of these reactions is briefly discussed.

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