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About This Item
Linear Formula:
(CH3)2CHCH(OH)CH(CH3)2
CAS Number:
Molecular Weight:
116.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-993-7
Beilstein/REAXYS Number:
1731593
MDL number:
Assay:
99%
InChI key
BAYAKMPRFGNNFW-UHFFFAOYSA-N
InChI
1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3
SMILES string
CC(C)C(O)C(C)C
assay
99%
Quality Level
bp
139-140 °C (lit.)
density
0.829 g/mL at 25 °C (lit.)
functional group
hydroxyl
Related Categories
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
98.6 °F - closed cup
flash_point_c
37 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Bart A C van As et al.
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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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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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Camptothecin (CPT), a quinolone alkaloid extracted from Camptotheca acuminata Decne, exhibits potential insecticidal activities against various insect species. Our previous studies have showed that CPT induced apoptosis in Spodoptera exigua Hübner cell line and inhibited the relaxation activity of topoisomerase
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