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150045

Sigma-Aldrich

2,4-Dimethyl-3-pentanol

99%

Synonym(s):

Diisopropylcarbinol

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About This Item

Linear Formula:
(CH3)2CHCH(OH)CH(CH3)2
CAS Number:
600-36-2
Molecular Weight:
116.20
Beilstein:
1731593
EC Number:
209-993-7
MDL number:
MFCD00008921
UNSPSC Code:
12352100
PubChem Substance ID:
24849002
NACRES:
NA.22

Assay

99%

refractive index

n20/D 1.425 (lit.)

bp

139-140 °C (lit.)

density

0.829 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3

InChI key

BAYAKMPRFGNNFW-UHFFFAOYSA-N

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Application

2,4-Dimethyl-3-pentanol was used as a proton source in the diastereoselective coupling with 2-substituted acrylate derivatives. It was used in the polymerization of 1,1′-(1,3-phenylene) diethanol (1,3-diol) and diisopropyl adipate.

Signal Word

Danger

Hazard Statements

H226,H302,H315,H318,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

98.6 °F - closed cup

Flash Point(C)

37 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The well-known dynamic kinetic resolution of secondary alcohols and esters was extended to secondary diols and diesters to afford chiral polyesters. This process is an example of iterative tandem catalysis (ITC), a polymerization method where the concurrent action of two
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Organic letters, 11(4), 879-882 (2009-01-28)
A mild, stereoselective method for the Ni-catalyzed synthesis of alpha-C-alkylglycosides is reported. This approach entails the reductive coupling of glycosyl bromides with activated alkenes at room temperature, with low alkene loading as an important feature. Diastereoselective coupling with 2-substituted acrylate

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