Production Method 1

138-86-3

80-27-3

Reaction Conditions

1.1 Reagents: Hydrochloric acid
2.1 -

Reference

Solvolytic displacement of alkyl halides by metal salts. Preparative procedures for allyl-, benzyl-, and tertiary alkyloxy derivatives using the zinc salts

Gurudutt, K. N.; et al, Tetrahedron, 1982, 38(12), 1843-6

Production Method 2

39864-10-3

80-27-3

Reaction Conditions

Reference

Solvolytic displacement of alkyl halides by metal salts. Preparative procedures for allyl-, benzyl-, and tertiary alkyloxy derivatives using the zinc salts

Gurudutt, K. N.; et al, Tetrahedron, 1982, 38(12), 1843-6

Production Method 3

98-55-5

80-27-3

Reaction Conditions

1.1 Catalysts: Tosyl chloride ;  1.5 h, rt
1.2 Reagents: Sodium hydroxide Solvents: Water ;  pH 7 - 8, rt

Reference

Discovery of a novel series of α-terpineol derivatives as promising anti-asthmatic agents: Their design, synthesis, and biological evaluation

Zhu, Wanping; et al, European Journal of Medicinal Chemistry, 2018, 143, 419-425

p-menth-1-en-8-yl propionate Raw materials

• 4-(1-chloro-1-methylethyl)-1-methylcyclohexene
• Limonene
• α-Terpineol

p-menth-1-en-8-yl propionate Preparation Products

• p-menth-1-en-8-yl propionate (80-27-3)

• 1. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?
  Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
• 2. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 3. Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines?
  Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
• 4. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 5. Fe3O4 nanoclusters highly dispersed on a porous graphene support as an additive for improving the hydrogen storage properties of LiBH4?
  Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361

• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Menthane monoterpenoids
• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Monoterpenoids Menthane monoterpenoids

• 7774-65-4(Propanoic acid,2-methyl-, 1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl ester)
• 2153-28-8(Butanoic acid,1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl ester)
• 14481-55-1(Pentanoic acid,1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl ester)
• 1142-85-4(Butanoic acid,3-methyl-, 1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl ester)
• 71648-35-6(Octanoic acid,1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl ester)
• 10581-37-0(()-α,α,4-trimethylcyclohex-3-ene-1-methyl acetate)
• 80-26-2(alpha-Terpinyl acetate)
• 4821-09-4(1-(isopropyl)-4-methylcyclohex-3-en-1-yl acetate)
• 170233-85-9(Butanedioic acid, 1-[1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl] ester)
• 8007-35-0(Terpineol, acetate)