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Propanedioic acid, 2-hexylidene-, also known as 2-hexylidenemalonate or 2-hexylidenemalonic acid, is an organic compound with the chemical formula C9H14O4. It is a colorless liquid with a molecular weight of 186.21 g/mol. Propanedioic acid,2-hexylidene- is a derivative of malonic acid, featuring a six-carbon alkyl chain (hexyl group) bridging the two carboxyl groups. It is used as an intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is essential to handle Propanedioic acid,2-hexylidene- with care, following proper safety protocols.

4360-85-4

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4360-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4360-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4360-85:
(6*4)+(5*3)+(4*6)+(3*0)+(2*8)+(1*5)=84
84 % 10 = 4
So 4360-85-4 is a valid CAS Registry Number.

4360-85-4SDS

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 hexylidene-malonic acid

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

1.5 Emergency phone number

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More Details:4360-85-4 SDS

4360-85-4Relevant articles and documents

Practical synthesis of (E)-α,β-unsaturated carboxylic acids using a one-pot hydroformylation/decarboxylative Knoevenagel reaction sequence

Kemme, Susanne T.,?mejkal, Tomá?,Breita, Bernhard

supporting information; experimental part, p. 989 - 994 (2009/05/27)

Combining the regioselective room temperature/ambient pressure hydroformylation and a modification of the Doebner-Knoevenagel reaction allowed for the development of an efficient, one-pot procedure for the synthesis of (E)-α,β-unsaturated carboxylic acids. The reaction proceeds under mild conditions, tolerates a variety of functional groups and gives (E)-α,β-unsaturated carboxylic acids in good yields and with excellent regio-and stereocontrol. The practicability of this process has been demonstrated by a short protecting group-free synthesis of the queen honeybee pheromones 9-ODA[( E)-9-oxodec-2-enoic acid] and 9-HDA[( E)-9-hydroxydec-2-enoic acid].

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