88808
(S)-(+)-1-Methoxy-2-propanol
≥98.5% (sum of enantiomers)
Synonym(s):
(S)-(+)-Propylene glycol 1-methyl ether
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About This Item
Empirical Formula (Hill Notation):
C4H10O2
CAS Number:
Molecular Weight:
90.12
UNSPSC Code:
12352112
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1718940
Assay:
≥98.5% (sum of enantiomers)
Form:
liquid
InChI
1S/C4H10O2/c1-4(5)3-6-2/h4-5H,3H2,1-2H3/t4-/m0/s1
SMILES string
COC[C@H](C)O
InChI key
ARXJGSRGQADJSQ-BYPYZUCNSA-N
assay
≥98.5% (sum of enantiomers)
form
liquid
optical activity
[α]20/D +22±2°, c = 10% in chloroform
refractive index
n20/D 1.403
density
0.921 g/mL at 20 °C (lit.)
functional group
ether, hydroxyl
Quality Level
Related Categories
Application
(S)-(+)-1-Methoxy-2-propanol can be used as a reactant to prepare:
- (S)-1-methoxypropan-2-yl 4-methylbenzenesulfonate by reacting with tosyl chloride in the presence of pyridine.
- Thiazolopyridine urea derivatives.
- Quinazoline derivatives as potential inhibitors of EGFR/HER-2 tyrosine kinases.
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Discovery of new quinazoline derivatives as irreversible dual EGFR/HER2 inhibitors and their anticancer activities-Part 1
D Debasis, et al.
Bioorganic & medicinal chemistry letters, 29(4), 591-596 (2019)
Thiazolopyridine ureas as novel antitubercular agents acting through inhibition of DNA gyrase B
K Manoj G, et al.
Journal of Medicinal Chemistry, 56(21), 8834-8848 (2013)
Stereocontrolled C (sp 3)-P bond formation with non-activated alkyl halides and tosylates
Yang C-T, et al.
Royal Society of Chemistry Advances, 7(40), 24652-24656 (2017)
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