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88808

Sigma-Aldrich

(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:
26550-55-0
Molecular Weight:
90.12
Beilstein:
1718940
MDL number:
MFCD01632588
UNSPSC Code:
12352112
PubChem Substance ID:
57653320
NACRES:
NA.22

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.)

SMILES string

COC[C@H](C)O

InChI

1S/C4H10O2/c1-4(5)3-6-2/h4-5H,3H2,1-2H3/t4-/m0/s1

InChI key

ARXJGSRGQADJSQ-BYPYZUCNSA-N

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.

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

91.4 °F - closed cup

Flash Point(C)

33 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

88808-BULK-F:
88808-1ML-F:
88808-5ML-F:
88808-VAR-F:

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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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)
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)
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)

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