26728-45-0

Basic information

• Product Name: isopropyl 3,7-dimethyloct-6-enoate
• Synonyms: isopropyl 3,7-dimethyloct-6-enoate;3,7-Dimethyl-6-octenoic acid 1-methylethyl ester
• CAS NO: 26728-45-0
• Molecular Formula: C₁₃H₂₄O₂
• Molecular Weight: 212.32846
• EINECS: 247-946-2
• Mol File: 26728-45-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 261°Cat760mmHg
• Flash Point: 80°C
• Appearance: /
• Density: 0.881g/cm³
• Vapor Pressure: 0.0119mmHg at 25°C
• Refractive Index: 1.443
• CAS DataBase Reference: isopropyl 3,7-dimethyloct-6-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: isopropyl 3,7-dimethyloct-6-enoate(26728-45-0)
• EPA Substance Registry System: isopropyl 3,7-dimethyloct-6-enoate(26728-45-0)

Safety Data

• Hazardous Substances Data: 26728-45-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H24O2/c1-10(2)7-6-8-12(5)9-13(14)15-11(3)4/h7,11-12H,6,8-9H2,1-5H3

Upstream product

• 40267-53-6 (E)-N,N-diethyl-3,7-dimethyl-2,6-octadienylamine 
• 67-63-0 isopropyl alcohol 
• 36392-06-0 3,7-dimethyl-6-octenoyl chloride 
• 152481-48-6 isopropyl 3,7-dimethyl-2ξ,6-octadienoate 
• 502-47-6 racemic citronellic acid 
• 3209-78-7 5,5-dimethoxy-pentan-2-one 
• 56422-95-8 ethyl-2-carbethoxy-3,7-dimethyl-oct-6-enoate 
• 86294-67-9 2-(Trimethylsilyl)ethansaeure-isopropylester 
• 152481-67-9 2-(1,5-Dimethyl-hex-4-enyl)-malonic acid 
• 152481-59-9 ethyl 2-ethoxycarbonyl-3-methyl-6,6-dimethoxy2-hexenoate 
• 152481-62-4 ethyl 2-ethoxycarbonyl-3-methyl-6,6-dimethoxyhexanoate 
• 106-23-0 3,7-dimethyl-oct-6-enal 

Relevant articles and documents

Rhodium-catalyzed asymmetric synthesis of β-branched esters from allylic amines

Allylic amines are converted to chiral, β-branched esters under rhodium catalysis in the presence of alcohol nucleophiles. Allylic amines with aliphatic and aromatic vinylic substituents are converted to ester products with excellent enantioselectivities in all cases. Several alcohol nucleophiles have been utilized in the reaction including 1° and 2° derivatives.

OZONOLYSIS OF ALKENES AND THE REACTIONS OF POLYFUNCTIONAL COMPOUNDS LIII.SYNTHESIS OF THE ESTERS OF 2,3-DIHYDRO DERIVATIVES OF TRI-, DI-, AND MONOPRENOIC ACIDS

The esters of the 2,3-dihydro derivatives of geranylgeranic, farnesylic, and geranic acids (di-, sesqui-, and monoterpenoid acids) were synthesized from the products from ozonolysis of 1,5,9-trimethyl-1E,5E,9E-cyclododecatriene.