629-72-1 Usage
Description
1-BROMOPENTADECANE, a clear colorless to pale yellow liquid after melting, is an organic compound with the molecular formula C15H31Br. It is characterized by its bromine atom attached to a long hydrocarbon chain, which contributes to its unique chemical properties and potential applications.
Uses
Used in Chemical Synthesis:
1-BROMOPENTADECANE is used as a reagent for the synthesis of (S)-eicos-(4E)-en-1-yn-3-ol, a bioactive component found in the marine sponge Cribrochalina vasculum. Its unique structure allows it to serve as a valuable intermediate in the creation of complex organic molecules, particularly those with potential biological activities.
Used in Monolayer Research:
1-BROMOPENTADECANE has been utilized in the investigation of mixed monolayers of deuterated palmitic acid (dPA) and deuterated stearic acid (dSA) at the air-water interface. Its incorporation into these monolayers provides insights into the behavior and properties of such systems, which can be crucial for understanding various phenomena at the molecular level and developing applications in materials science and surface chemistry.
While the provided materials do not explicitly mention other industries where 1-BROMOPENTADECANE might be used, its chemical properties and applications in chemical synthesis and monolayer research suggest that it could potentially be relevant in fields such as pharmaceuticals, materials science, and environmental science. Further research and development could reveal additional uses for this versatile compound.
Check Digit Verification of cas no
The CAS Registry Mumber 629-72-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 629-72:
(5*6)+(4*2)+(3*9)+(2*7)+(1*2)=81
81 % 10 = 1
So 629-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H31Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h2-15H2,1H3
629-72-1Relevant articles and documents
Chemoenzymatic synthesis of (S)-eicos-(4E)-en-1-yn-3-ol, the cytotoxic principle of the marine sponge, Cribrochalina vasculum
Sharma, Anubha,Chattopadhyay, Subrata
, p. 2635 - 2639 (1998)
An efficient enantioselective synthesis of the title compound I was developed from the versatile chiron 1-tert-butyldimethylsilylpenta-1,4-diyn- 3-ol 2. The chiron, in turn, was prepared via a combination of lipase catalyzed acylation-alcoholysis protocol. Protection of its hydroxy group, alkylation with a suitable bromide and subsequent functionalization gave (S)- I with high enantiomeric purity.
Photolytic generation of carbon radicals from Barton esters: Recent developments
Barton,Jaszberenyi,Tang
, p. 3381 - 3384 (2007/10/02)
O-Acyl derivatives of N-hydroxy-2-thiopyridone can be photolysed with suitable commercial visible-light lamps to give reactions with very short half-lives (down to 20 s) at 0° C or room temperature.
Quantum Yields in the Photochemically Induced Radical Chemistry of Acyl Derivatives of Thiohydroxamic Acids
Barton, Derek H. R.,Blundell, Paul,Jaszberenyi, Joseph Cs.
, p. 6937 - 6942 (2007/10/02)
Acyl derivatives of N-hydroxyquinazoline-4-thiones are a novel source of disciplined carbon radicals.Quantum yield determination reveals that photolysis of these compounds initiates radical chains, resulting in quantum yields up to φ = 60.Comparative studies with acyl derivatives of N-hydroxy-2-thiopyridone show that the quinazoline derivatives are more light-sensitive than the thiopyridone compounds.The carbon radicals thus formed from the former can be trapped selectively, without the formation of rearranged products (i.e. without the competition of the radicophilic thiocarbonyl group of the starting material with the radical trap).
