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4-(Heptyloxy)-3-methoxybenzaldehyde is an organic compound with the molecular formula C16H24O3. It is a derivative of benzaldehyde, featuring a heptyloxy group (a seven-carbon alkyl chain attached to an oxygen atom) at the 4-position and a methoxy group (a single-carbon alkyl chain attached to an oxygen atom) at the 3-position. This aromatic aldehyde is characterized by its distinct chemical structure, which contributes to its unique properties and potential applications in various fields, such as pharmaceuticals, fragrances, and chemical research. The compound's molecular weight is 264.36 g/mol, and it is likely to exhibit specific physical and chemical properties due to its functional groups and molecular arrangement.

5438-59-5

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5438-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5438-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5438-59:
(6*5)+(5*4)+(4*3)+(3*8)+(2*5)+(1*9)=105
105 % 10 = 5
So 5438-59-5 is a valid CAS Registry Number.

5438-59-5SDS

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 N-Formyl-3-methoxymorpholin

1.2 Other means of identification

Product number -
Other names 3-methoxy-4-formylmorpholine

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:5438-59-5 SDS

5438-59-5Relevant academic research and scientific papers

Structural characterization of vanillin derivatives with long alkyl chain and investigation of their electrochemical and thermal properties

Tümer, Mehmet,Tümer, Ferhan,K?se, Muhammet

, (2020)

This manuscript describes the synthesis, characterization and thermal properties of the two vanillin derivatives containing a long alkyl chain. Two vanillin derivatives 4-(heptyloxy)-3-methoxybenzaldehyde (L1) and 4-(decyloxy)-3-methoxybenzalde

Synthesis and liquid crystalline properties of a new homologous series of 4,5-disubstituted 2H-[1,2,3]-triazoles via azide-chalcone oxidative cycloaddition reaction

Sowmya,Rai, K. M. Lokanatha

, p. 764 - 768 (2017/07/07)

A new homologous series of 4,5-disubstituted 2H-[1,2,3]-triazole derivatives were synthesized from chalcones and sodium azide via oxidative cycloaddition reaction; CuI was used as catalyst. Flexibility in the synthesized molecules was provided by attaching straight alkoxy chains. The synthesized compounds were characterized by elemental analysis, and 1HNMRand 13CNMRand LC-MS spectroscopies . The stability and range of the mesophases increased with the length of the chain on the triazoles. The melting point, transition temperatures, and enantiotropic liquid crystal morphologies were determined by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM) equipped with a hot stage. Journal compilation

Synthesis and characterization of new homologous series of unsymmetrical liquid crystalline compounds based on chalcones and 3, 5-disubstituted isoxazoles

Sowmya,Lokanatha Rai

, p. 67 - 73 (2017/01/24)

Two homologous series of unsymmetrical alkylated chalcones and 3,5-diaryl isoxazoles, consisting of 20 members, with various n-alkyl bromides (n=2?7, 10, 12, 14, 16) have been synthesized and studied for their liquid crystalline property. Simple strategy was employed to achieve the target materials. Flexibility in the synthesized molecules is provided by attaching straight alkoxy chains, where one terminal group is fixed and other terminal group is varied. The synthesized compounds were characterized on the basis of Mass, IR and NMR spectroscopy. The stability and the range of the mesophases increased with the length of the chain on the isoxazoles. The melting point, transition temperatures and enantiotropic liquid crystal morphologies were determined by polarizing optical microscopy (POM) in conjunction with a hot stage and by differential scanning calorimetry (DSC). [Figure not available: see fulltext.]

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