2624-01-3 Usage
Description
A-BROMOHEPTANOIC ACID, with the molecular formula C7H13BrO2, is a carboxylic acid featuring a bromine atom attached to the alpha carbon. It is a member of the fatty acids class and is recognized for its colorless crystalline solid form and strong, unpleasant odor. This chemical compound is widely utilized in organic synthesis and serves as a reagent in various chemical reactions. Its applications extend to the production of pharmaceuticals, agrochemicals, and other organic compounds, where it functions as an intermediate in the synthesis of additional compounds. Moreover, A-BROMOHEPTANOIC ACID has garnered interest for its potential pharmaceutical applications, attributed to its antibacterial and antifungal properties.
Uses
Used in Pharmaceutical Production:
A-BROMOHEPTANOIC ACID is used as a key intermediate for the synthesis of various pharmaceuticals, given its unique chemical structure and reactivity.
Used in Agrochemical Production:
A-BROMOHEPTANOIC ACID is used as a precursor in the development of agrochemicals, contributing to the creation of effective compounds for agricultural applications.
Used in Organic Synthesis:
A-BROMOHEPTANOIC ACID is used as a reagent in organic synthesis, facilitating the formation of a range of organic compounds through its reactive bromine atom.
Used in Research and Development:
A-BROMOHEPTANOIC ACID is used as a research compound for studying its antibacterial and antifungal properties, exploring its potential as a pharmaceutical agent in treating infections.
Used in Chemical Reactions:
A-BROMOHEPTANOIC ACID is used as a reactant in various chemical reactions, taking advantage of its bromine atom for functional group transformations and the formation of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 2624-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2624-01:
(6*2)+(5*6)+(4*2)+(3*4)+(2*0)+(1*1)=63
63 % 10 = 3
So 2624-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13BrO2/c1-2-3-4-5-6(8)7(9)10/h6H,2-5H2,1H3,(H,9,10)
2624-01-3Relevant articles and documents
Synthesis and Surface-Active Properties of a Homologous Series of Star-Like Triple-Chain Anionic Surfactants Derived from 1,1,1-Tris(hydroxymethyl)ethane
Li, Xu,Xing, Fenglan,Xu, Qun,Sun, Xiaolong,Wang, Yuping,Wang, Liyan,Wang, Pinglang
, p. 129 - 135 (2016/01/09)
A novel homologous series of trimeric anionic surfactants, 3C n TE3CNa (where n is a fatty acid chain length of 7, 10, or 12), with three hydrocarbon chains and three carboxylate heads connected via tri-etheric bonds were synthesized from long-chain α-bromo fatty acids and a triol, 1,1,1-tris(hydroxymethyl)ethane. The obtained trimeric carboxylic acids were esterified and purified by silica gel column chromatography, then hydrolyzed with dilute sodium hydroxide solution to form a series of trimeric carboxylate surfactant products. All prepared compounds were analyzed by IR, 1H NMR, and 13C NMR spectroscopy to confirm their chemical structures. Their surface-active properties were investigated. The critical micelle concentrations (cmc) of 3C n TE3CNa were in the range of 0.12-0.71 mmol/L, and the surface tensions at the cmc (γ cmc) were 29.3-34.8 mN/m.
Mesoionic 5-alkyl-1,3-dithiolium-4-thiolates: Synthesis and brine shrimp toxicity
De Almeida, Paulo Afonso,Da Silva, Tania Maria Sarmento,Echevarria, Aurea
, p. 593 - 600 (2007/10/03)
A series of twelve 1,3-dithiolium-4-thiolate mesoionic compounds were synthesized and characterized. The synthetical approach starting from α-bromoalkanoic acids to obtain the corresponding 2-N-morpholino-dithiocarbamoyl-carboxylic acids that by on-pot reaction with carbon disulfide and acetic anhydride in triethylamine formed not isolate intermediates, 1,3-dithiolium-4-olates. After, the 2-N-morpholino-5-alkyl-1,3-dithiolium-4-thiolates were obtained by retro 1,3-dipolar addition reactions. The alkyl moiety linked to C-5 of heterocyclic ring permitted the increase of the hydrophobic character and this effect was evaluated on Artemia salina lethality. The results indicated a bell-shaped relationship between the number of carbon of side chain in mesoionic derivatives and LD50 in brine shrimp toxicity assays.
