142-94-9 Usage
Description
2-Bromostearic acid, a member of the stearic acid class, is a chemical compound distinguished by the presence of a bromine atom. It is recognized for its capacity to alter the physical and chemical properties of materials, which is beneficial across a variety of industrial applications. As a versatile building block, 2-Bromostearic acid is instrumental in the synthesis of a broad spectrum of organic compounds and serves as a precursor in the preparation of numerous chemical products, making it a significant component in the manufacturing of a diverse array of commercial and industrial goods.
Uses
Used in Specialty Chemicals Production:
2-Bromostearic acid is utilized as a key component in the production of specialty chemicals, where its unique structure and reactivity contribute to the development of high-value products with specific properties tailored for particular applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Bromostearic acid serves as a crucial intermediate in the synthesis of various drugs, leveraging its chemical properties to enhance the efficacy and functionality of medicinal compounds.
Used in Surfactants and Detergents:
2-Bromostearic acid is employed as a component in the formulation of surfactants and detergents, where it helps to improve the cleaning power and stability of these products, as well as their ability to work under different conditions.
Used in Synthesis of Other Organic Compounds:
As a precursor, 2-Bromostearic acid is used in the synthesis of a wide range of other organic compounds, providing a foundation for the creation of new chemical entities with diverse applications in various industries.
Used in Manufacturing of Commercial and Industrial Products:
2-Bromostearic acid plays a significant role in the manufacturing process of a multitude of commercial and industrial products, where its ability to modify material properties is harnessed to achieve desired characteristics and performance standards.
Check Digit Verification of cas no
The CAS Registry Mumber 142-94-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 142-94:
(5*1)+(4*4)+(3*2)+(2*9)+(1*4)=49
49 % 10 = 9
So 142-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H35BrO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(19)18(20)21/h17H,2-16H2,1H3,(H,20,21)/t17-/m0/s1
142-94-9Relevant articles and documents
Hydroxy fatty acids for the delivery of dideoxynucleosides as anti-HIV agents
Gangadhara, Kishore Lingam,Lescrinier, Eveline,Pannecouque, Christophe,Herdewijn, Piet
, p. 817 - 820 (2014)
A series of α- and β-carboxylated phospholipid prodrugs of dideoxy nucleosides have been synthesized and evaluated against HIV. An increase in biological effect with a factor of 500 has only been observed for the adenine nucleoside, which suggests that this prodrug approach is base specific.
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.
Synthesis of (2S,2'R,3R,4E,8E)-N-2'-Hydroxyoctadecanoyl-1-O-(β-D-glucopyranosyl)-9-methyl-4,8-sphingadienine (Pen III), a Cerebroside Isolated from Penicillium funiculosum as the Fruiting Inducer against Schizophyllum commune
Abe, Tatsuichirou,Mori, Kenji
, p. 1671 - 1674 (2007/10/02)
(2S,2'R,3R,4E,8E)-N-2'-Hydroxyoctadecanoyl-1-O-(β-D-glucopyranosyl)-9-methyl-4,8-sphingadienine (Pen III), a cerebroside isolated from Penicillium funiculosum A-1 as the fruiting inducer against Basidiomycete Schizophyllum commune, was synthesized by starting from D-glucose, L-serine, homoprenyl acetate and stearic acid.
