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727296

Sigma-Aldrich

(S)-1-Methoxy-2-propylamine

ChiPros®, produced by BASF, 99%

Synonym(s):

(S)-2-Amino-1-methoxypropane

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5 G
$133.00
25 G
$349.00

$133.00

Available to ship onApril 22, 2025Details

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5 G
$133.00
25 G
$349.00

About This Item

Empirical Formula (Hill Notation):
C4H11NO
CAS Number:
99636-32-5
Molecular Weight:
89.14
Beilstein/REAXYS Number:
5725728
MDL number:
MFCD01075730
UNSPSC Code:
12352112
PubChem Substance ID:
329764313
NACRES:
NA.22

$133.00

Available to ship onApril 22, 2025Details

Request a Bulk Order

Quality Level

100

assay

≥98.5% (GC)
99%

form

liquid

optical purity

enantiomeric excess: ≥99.5%

functional group

amine
ether

SMILES string

COC[C@H](C)N

InChI

1S/C4H11NO/c1-4(5)3-6-2/h4H,3,5H2,1-2H3/t4-/m0/s1

InChI key

NXMXETCTWNXSFG-BYPYZUCNSA-N

Related Categories

Application

(S)-1-Methoxy-2-propylamine can be used:
  • As an intermediate in the synthesis of piperazinebenzylamine based human MC4 receptor antagonists.[1]
  • To prepare imidazopyrimidine derivatives as potent p38 MAP kinase inhibitors.[2]
  • In the synthesis of a marine natural product nhatrangin A.[3]

Legal Information

ChiPros is a registered trademark of BASF SE

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

47.3 °F

flash_point_c

8.5 °C

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL8394
BCCK1005
BCCH2155
BCCH9738
BCCC3386

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Formal enantioselective synthesis of nhatrangin A
Feuillastre S, et al.
Organic & Biomolecular Chemistry, 18(10), 1949-1956 (2020)
Optimization of piperazinebenzylamines with a N-(1-methoxy-2-propyl) side chain as potent and selective antagonists of the human melanocortin-4 receptor
Pontillo J, et al.
Bioorganic & medicinal chemistry letters, 15(20), 4615-4618 (2005)
Imidazopyrimidines, potent inhibitors of p38 MAP kinase
Rupert KC, et al.
Bioorganic & Medicinal Chemistry Letters, 13(3), 347-350 (2003)

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