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541486

2,6-Dimethyl-4-heptanol

80%

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About This Item

Linear Formula:
CH3CH(CH3)CH2CH(OH)CH2CH(CH3)CH3
CAS Number:
108-82-7
Molecular Weight:
144.25
EC Number:
203-619-6
MDL number:
MFCD00008944
UNSPSC Code:
12352100
PubChem Substance ID:
24878539
NACRES:
NA.22

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assay

80%

refractive index

n20/D 1.423 (lit.)

bp

178 °C (lit.)

density

0.809 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CC(C)CC(O)CC(C)C

InChI

1S/C9H20O/c1-7(2)5-9(10)6-8(3)4/h7-10H,5-6H2,1-4H3

InChI key

HXQPUEQDBSPXTE-UHFFFAOYSA-N

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1 of 4

This Item
150045307963CDS001248
2,6-Dimethyl-4-heptanol 80%

Sigma-Aldrich

541486

2,6-Dimethyl-4-heptanol

2,4-Dimethyl-3-pentanol 99%

Sigma-Aldrich

150045

2,4-Dimethyl-3-pentanol

2,6-Dimethyl-5-heptenal technical grade, 80%

Sigma-Aldrich

307963

2,6-Dimethyl-5-heptenal

4-Ethynyl-2,6-dimethyl-4-heptanol AldrichCPR

Sigma-Aldrich

CDS001248

4-Ethynyl-2,6-dimethyl-4-heptanol

assay

80%

assay

99%

assay

80%

assay

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

refractive index

n20/D 1.423 (lit.)

refractive index

n20/D 1.425 (lit.)

refractive index

n20/D 1.444 (lit.)

refractive index

-

bp

178 °C (lit.)

bp

139-140 °C (lit.)

bp

116-124 °C/100 mmHg (lit.)

bp

-

density

0.809 g/mL at 25 °C (lit.)

density

0.829 g/mL at 25 °C (lit.)

density

0.879 g/mL at 25 °C

density

-

functional group

hydroxyl

functional group

hydroxyl

functional group

aldehyde

functional group

-

Application

2,6-Dimethyl-4-heptanol may be used in the preparation of the protected β-hydroxybutyrates.[1] It may also be used as a hydrogen donor during the dynamic kinetic resolution (DKR) of various diols,[2] monoprotected diols and the protected hydroxy aldehydes.[3]

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

150.8 °F - closed cup

flash_point_c

66 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ7199
MKCW5860
MKCR5741
MKCL4342
MKCD8230

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Dynamic kinetic resolution of secondary alcohols by enzyme?metal combinations in ionic liquid.
Kim MJ, et al.
Green Chemistry, 6(9), 471-474 (2004)
Mahn Joo Kim et al.
Current opinion in biotechnology, 13(6), 578-587 (2002-12-17)
The combination of enzyme and metal catalysis is described as a useful method for the synthesis of optically active compounds. A key feature of this new methodology is the use of metal catalysts for the in situ racemization of enzymatically
Lipase/ruthenium-catalyzed dynamic kinetic resolution of hydroxy acids, diols, and hydroxy aldehydes protected with a bulky group.
M J Kim et al.
The Journal of organic chemistry, 66(13), 4736-4738 (2001-06-26)

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