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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide

(R)-2-isopropyl-5-methylhexanol synthesis

5synthesis methods
Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propen-1-yl)-, ethyl ester, (1R,3S)-

41641-26-3
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(R)-2-isopropyl-5-methylhexanol

41884-28-0
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-

Yield:-

Steps:

Multi-step reaction with 3 steps
1: BF3*OEt2 / heptane / 2 h / 70 °C / other Lewis acids
2: 86 percent / H2 / PtO2
3: 87 percent / LiAlH4

References:

Suzukamo, Gohfu;Fukao, Masami;Tamura, Mitsuhisa [Tetrahedron Letters,1984,vol. 25,# 15,p. 1595 - 1598]

498-16-8 Synthesis
LAVANDULOL

498-16-8
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(R)-2-isopropyl-5-methylhexanol

41884-28-0
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References
Hexanoic acid, 5-methyl-2-(1-methylethyl)-, ethyl ester, (R)- (9CI)

87017-28-5
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(R)-2-isopropyl-5-methylhexanol

41884-28-0
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References
(-)-DIHYDROCARVYL ACETATE

20777-39-3
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(R)-2-isopropyl-5-methylhexanol

41884-28-0
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References
3-Hexenoic acid, 5-methyl-2-(1-methylethenyl)-, ethyl ester, [R-(E)]- (9CI)

87068-42-6
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(R)-2-isopropyl-5-methylhexanol

41884-28-0
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References