16900-59-7

Basic information

• Product Name: 4-Decynoic acid
• Synonyms: 4-Decynoic acid
• CAS NO: 16900-59-7
• Molecular Formula: C₁₀H₁₆O₂
• Molecular Weight: 168.23
• Mol File: 16900-59-7.mol

Chemical Properties

• Melting Point: 28.5°C (estimate)
• Boiling Point: 325.33°C (rough estimate)
• Appearance: /
• Density: 1.0066 (rough estimate)
• Refractive Index: 1.4036 (estimate)
• CAS DataBase Reference: 4-Decynoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Decynoic acid(16900-59-7)
• EPA Substance Registry System: 4-Decynoic acid(16900-59-7)

Safety Data

• Hazardous Substances Data: 16900-59-7(Hazardous Substances Data)

Upstream product

• 99861-83-3 oct-2-ynyl-malonic acid 
• 94253-44-8 2-(Dec-4-inoyl)-cyclooctanon 
• 110-53-2 1-Bromopentane 
• 6089-09-4 4-pentynoic acid 
• 18495-27-7 1-bromooct-2-yne 
• 92860-92-9 oct-2-ynyl-malonic acid diethyl ester 
• 90972-95-5 Dec-4-inoylchlorid 
• 5390-04-5 pent-1-yn-5-ol 
• 62992-46-5 1-(tetrahydropyranyloxy)-4-pentyn 
• 77022-43-6 4-Decyn-1-yl tetrahydropyranyl ether 

Downstream Products

• 93156-56-0 2-(Dec-4-inoyl)-cyclohexanon 
• 118267-99-5 (4R,5S)-3-((Z)-(R)-2-Hydroxy-dec-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one 
• 118267-98-4 (4R,5S)-3-((Z)-Dec-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one 
• 100428-42-0 2(R)-<(tert-butyldiphenylsilyl)oxy>dec-4(Z)-enal 
• 128891-59-8 (4R,5S)-3-[(Z)-(R)-2-(tert-Butyl-diphenyl-silanyloxy)-dec-4-enoyl]-4-methyl-5-phenyl-oxazolidin-2-one 
• 126617-76-3 (2R,4Z)-2(tert-Butyldiphenylsiloxy)-4-decen-1-ol 
• 57602-94-5 (E)-4-decenoic acid 
• 505-90-8 (Z)-dec-4-enoic acid 

Relevant articles and documents

(Z)-N-(4-Decenoyl)homoserine lactone, a new quorum-sensing molecule, produced by endobacteria associated with Mortierella alpina A-178

N-Acylhomoserine lactones (AHLs) are the conserved quorum-sensing signal molecules in Gram-negative bacteria. (Z)-N-(4-Decenoyl)homoserine lactone (1), a new AHL, was isolated from the culture broth of the fungus Mortierella alpina A-178 harboring bacterial endosymbionts, called endobacteria. The structure and absolute configuration of 1 were elucidated by EI-MS, chemical synthesis, and chiral GC analysis. The compound induced the expression of a QS-regulated reporter gene in Agrobacterium tumefaciens NTL4, although its activity was lower than that of N-decanoylhomoserine lactone (6).

A Simple, General Diastereoselective Synthesis of 5-Hydroxyalkylbutan-4-olides

cis- and trans-Hex-4-enoic acids and their 6-n-propyl and n-butyl derivatives, when treated with a 1.1 molar excess of m-chloroperbenzoic acid and Amberlyst-15 as catalyst in CH2Cl2 at 20 deg C, gave the corresponding threo- and erythro-5-hydroxyalkylbutan-4-olides in quantitative yields.