17108-71-3

Basic information

• Product Name: 9(10)-bromostearic acid mixed isomers
• Synonyms: 9(10)-bromostearic acid;9(10)-Bromooctadecanoic acid;9(10)-BROMOSTEARIC ACID MIXED ISOMERS
• CAS NO: 17108-71-3
• Molecular Formula: C₁₈H₃₅BrO₂
• Molecular Weight: 363.37
• Mol File: 17108-71-3.mol
• Article Data: 8

Chemical Properties

• Storage Temp.: 2-8°C
• CAS DataBase Reference: 9(10)-bromostearic acid mixed isomers(CAS DataBase Reference)
• NIST Chemistry Reference: 9(10)-bromostearic acid mixed isomers(17108-71-3)
• EPA Substance Registry System: 9(10)-bromostearic acid mixed isomers(17108-71-3)

Safety Data

• Hazardous Substances Data: 17108-71-3(Hazardous Substances Data)

Upstream product

• 57-11-4 stearic acid 
• 7726-95-6 bromine 

Downstream Products

• 102874-95-3 2-Benzaminooxy-octadecansaeure-⁽¹⁾ 
• 5782-80-9 2-amino-octadecanoic acid 
• 7152-35-4 Diethyl-α-ethoxycarbonylheptadecylphosphonat 
• 67491-95-6 2-(2-Hydroxyethylamino)octadecanoic acid 
• 14663-11-7 methyl trans-2-octadecenoate 
• 2420-35-1 2-hydroxyoctadecanoic acid methyl ester 
• 629-22-1 2-hydroxystearic acid 
• 26633-48-7 (2R)-2-hydroxyoctadecanoic acid 
• 26531-80-6 (S)-2-hydroxyoctadecanoic acid 
• 5340-63-6 octadec-2-enoic acid 
• 5340-56-7 ethyl 2-bromostearoate 
• 96579-02-1 2-anilino-octadecanoic acid 
• 65164-70-7 α-iodostearic acid 
• 2825-79-8 (E)-2-octadecenoic acid 

Relevant articles and documents

Hydroxy fatty acids for the delivery of dideoxynucleosides as anti-HIV agents

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

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

(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.