83447-87-4

Basic information

• Product Name: 10-(2-hexylcyclopropyl)decanoic acid
• Synonyms: 10-(2-Hexylcyclopropyl)decanoic acid; 11,12-Methyleneoctadecanoic Acid; 19625-10-6; cyclopropanedecanoic acid, 2-hexyl-
• CAS NO: 83447-87-4
• Molecular Formula: C₁₉H₃₆O₂
• Molecular Weight: 296.4879
• Mol File: 83447-87-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 408.7°C at 760 mmHg
• Flash Point: 180°C
• Density: 0.923g/cm³
• Vapor Pressure: 8E-08mmHg at 25°C
• Refractive Index: 1.47
• CAS DataBase Reference: 10-(2-hexylcyclopropyl)decanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 10-(2-hexylcyclopropyl)decanoic acid(83447-87-4)
• EPA Substance Registry System: 10-(2-hexylcyclopropyl)decanoic acid(83447-87-4)

Safety Data

• Hazardous Substances Data: 83447-87-4(Hazardous Substances Data)

Upstream product

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• 73010-80-7 1-tetrahydropyranyloxyundecyl-11-triphenylphosphonium bromide 
• 133494-60-7 (1R,2S)-1-butyroyloxymethyl-2-formylcyclopropane 
• 133494-56-1 cis-(1R,2S)-1-butyryloxymethyl-2-hydroxymethylcyclopropane 
• 21406-61-1 pentyltriphenylphosphonium bromide 
• 252009-75-9 (1R,2S)-2-hexyl-1-(10'-hydroxydec-1'-yl)cyclopropane 
• 629-05-0 n-octyne 
• 212953-98-5 (+/-)-2-hexylcycloprop-2-ene-1-carboxylic acid 
• 131295-27-7 ethyl 1-hexylcyclopropen-3-ylcarboxylic ester 
• 678195-53-4 (4S)-4-benzyl-3-[(1S)-2-hexylcycloprop-2-ene-1-carbonyl]oxazolidin-2-one 

Relevant articles and documents

Cyclopropanation by Gold- or Zinc-Catalyzed Retro-Buchner Reaction at Room Temperature

Through the design of a second generation of more reactive 7-substituted 1,3,5-cycloheptatrienes, a room-temperature gold(I)-catalyzed retro-Buchner-cyclopropanation sequence and the first zinc(II)-catalyzed version of this process, which uses inexpensive

Total syntheses of cis-cyclopropane fatty acids: Dihydromalvalic acid, dihydrosterculic acid, lactobacillic acid, and 9,10-methylenehexadecanoic acid

cis-Cyclopropane fatty acids (cis-CFAs) are widespread constituents of the seed oils of subtropical plants, membrane components of bacteria and protozoa, and the fats and phospholipids of animals. We describe a systematic approach to the synthesis of enan

The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues

(11R, 12S)-Lactobacillic acid (1) has been prepared either from D- mannitol by asymmetric cyclopropanation or from cis-cyclopropane-1, 2- dimethanol by enzymatic desymmetrisation. The syntheses of (l1S 12R)- lactobacillic acid (2) and (1R, 2S) 1- (3'-methoxycarbonylpropyl)-2- octadecylcyclopropane (26) and related analogues (27 and 28) have also been achieved.