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α-Formylcaprylate, also known as 2-formylcaprylic acid or 2-formyloctanoic acid, is an organic compound with the chemical formula C8H14O3. It is a derivative of caprylic acid, an 8-carbon saturated fatty acid, with a formyl group (CHO) attached to the second carbon atom. α-formylcaprylate is a colorless liquid with a pungent odor and is soluble in organic solvents. α-Formylcaprylate is used as a chemical intermediate in the synthesis of various pharmaceuticals, fragrances, and other specialty chemicals. It is also known for its potential antimicrobial properties and has been studied for its ability to inhibit the growth of certain bacteria and fungi.

86654-32-2

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86654-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86654-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,5 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86654-32:
(7*8)+(6*6)+(5*6)+(4*5)+(3*4)+(2*3)+(1*2)=162
162 % 10 = 2
So 86654-32-2 is a valid CAS Registry Number.

86654-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name α-formylcaprylate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:86654-32-2 SDS

86654-32-2Relevant academic research and scientific papers

A supramolecular catalyst for the decarboxylative hydroformylation of α,β-unsaturated carboxylic acids

Smejkal, Tomas,Breit, Bernhard

, p. 3946 - 3949 (2008/12/23)

(Chemical Equation Presented) Head 'em up, move 'em out, aldehyde! A catalytic transformation of α,β-unsaturated carboxylic acids into aldehydes through a hydroformylation-decarboxylation process has been developed (see scheme; Do = donor ligand, FG1 and FG2 = complementary functional groups). The reaction proceeds at mild conditions, tolerates many functional groups, and liberates CO2 as the only stoichiometric by-product.

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