2082-76-0

Basic information

• Product Name: DECANOIC ANHYDRIDE
• Synonyms: CAPRIC ANHYDRIDE;DECANOIC ANHYDRIDE;N-DECANOIC ANHYDRIDE;N-CAPRIC ANHYDRIDE;n-capricanhtdride;CAPRIC ANHYDRIDE (C10:0);n-decylic anhydride;Bis(decanoic acid)anhydride
• CAS NO: 2082-76-0
• Molecular Formula: C₂₀H₃₈O₃
• Molecular Weight: 326.51
• EINECS: 218-213-4
• Mol File: 2082-76-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 24-25 °C(lit.)
• Boiling Point: 125-140 °C0.05 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: Colorless to light yellow/Melting Solid
• Density: 0.886 g/mL at 25 °C(lit.)
• Vapor Pressure: 2.22E-06mmHg at 25°C
• Refractive Index: n20/D 1.44(lit.)
• Storage Temp.: −20°C
• Solubility: chloroform: soluble100mg/mL, clear, colorless to light yellow
• CAS DataBase Reference: DECANOIC ANHYDRIDE(CAS DataBase Reference)
• NIST Chemistry Reference: DECANOIC ANHYDRIDE(2082-76-0)
• EPA Substance Registry System: DECANOIC ANHYDRIDE(2082-76-0)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-27-36/37/39-45
• RIDADR: UN 3261 8/PG 2
• WGK Germany: 3
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 2082-76-0(Hazardous Substances Data)

Usage

Chemical Properties

Colorless to light yellow low melting solid

Uses

Decanoic anhydride was used in the synthesis of 2-deoxy-2-p-methoxybenzylimideneaminio-1,3,4,6-tetra-O-decanoyl-D-glucopyranose.

InChI:InChI=1/C20H38O3/c1-3-5-7-9-11-13-15-17-19(21)23-20(22)18-16-14-12-10-8-6-4-2/h3-18H2,1-2H3

Upstream product

• 112-31-2 caprinaldehyde 
• 75-98-9 Trimethylacetic acid 
• 112-13-0 n-decanoyl chloride 
• 334-48-5 1-decanoic acid 
• 535-80-8 3-chlorobenzoate 
• 112-30-1 1-Decanol 
• 538-75-0 dicyclohexyl-carbodiimide 
• 111-66-0 oct-1-ene 
• 56-23-5 tetrachloromethane 
• 506-68-3 bromocyane 
• 108-24-7 acetic anhydride 

Downstream Products

• 124-11-8 non-1-ene 
• 205034-08-8 Decanoic acid 3-formyl-4-nitro-phenyl ester 
• 341925-62-0 3-(N-tert-butoxycarbonylamino)-5-(N'-decanoylamino)benzoic acid ethyl ester 
• 16899-02-8 7-hydroxypalmitic acid 
• 1401415-48-2 2',3'-bis-O-decanoyl-5'-deoxy-5'-[(N-methylcarbamoyl)amino]-N⁶-(N-phenylcarbamoyl)-adenosine 
• 57794-08-8 (1S,2S)-trans-1,2-Cyclohexanediol 
• 1072-86-2 (1R,2R)-trans-1,2-cyclohexanediol 
• 1532564-76-3 C₁₆H₃₀O₃ 
• 1256842-53-1 C₁₂H₂₁⁽²⁾H₂NO₃ 
• 109760-77-2 L-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol 

Relevant articles and documents

Alcohol cross-coupling for the kinetic resolution of diols via oxidative esterification

We present an organocatalytic C-O-bond cross-coupling strategy to kinetically resolve racemic diols with aromatic and aliphatic alcohols, yielding enantioenriched esters. This one-pot protocol utilizes an oligopeptide multicatalyst, m-CPBA as the oxidant, and N,N-diisopropylcarbodiimide as the activating agent. Racemic acyclic diols as well as trans-cycloalkane-1,2-diols were kinetically resolved, achieving high selectivities and good yields for the products and recovered diols.

STRUCTURED PHOSPHOLIPIDS

A method of treating a patient in need of therapy for a disease in which cyokines have become dysregulated, or are otherwise capable of modulation to provide therapeutic benefit, is provided comprising administering to that patient a therapeutically effective dose of a phospholipid comprising a phosphatidyl group esterifed with one or more fatty acyl groups, characterised in that the phospholipid has at least one fatty acyl group at the sn-1 and/or sn-2 position of the phosphatidyl group, the fatty acyl group being selected from the group consisting of γ-linolenoyl, dihomo-γ-linolenoyl acid and arachidonoyl.