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25414-22-6,MFCD00003227
Catalog No.:AA003HHH
25414-22-6 | 2-METHOXYFURAN
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1g
>97.0%(GC)
1 week  
$105.00
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5g
>97.0%(GC)
1 week  
$279.00
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  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HHH
Chemical Name:
2-METHOXYFURAN
CAS Number:
25414-22-6
Molecular Formula:
C5H6O2
Molecular Weight:
98.0999
MDL Number:
MFCD00003227
IUPAC Name:
2-methoxyfuran
InChI:
InChI=1S/C5H6O2/c1-6-5-3-2-4-7-5/h2-4H,1H3
InChI Key:
OXCGHDNCMSOEBZ-UHFFFAOYSA-N
SMILES:
COc1ccco1
EC Number:
246-953-8
UNII:
25Y8I1P35T
Properties
Computed Properties
 
Complexity:
54  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
98.037g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
98.101g/mol
Monoisotopic Mass:
98.037g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
22.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.4  

Synonyms
 
2-methoxyfuran 
2-Methoxyfuran 
Furan,2-methoxy- 
EINECS 246-953-8 
PubChem19998 
ACMC-209gjs 
2-Methoxyfuran, 97% 
AC1L3KYH 
2-Furyl methyl ether # 
AC1Q57UG 
CTK1A4910 
DTXSID00180078 
25414-22-6 
ZINC2242715 
ANW-25718 
GEO-02985 
AKOS015912861 
FCH1116469 
ACM25414226 
NCGC00166235-01 
CC-11235 
SC-21425 
AB1004374 
Furan, 2-methoxy- 
DB-008218 
TC-114463 
FT-0612850 
M0936 
C-29909 
J-015986 
I14-49073 
InChI=1/C5H6O2/c1-6-5-3-2-4-7-5/h2-4H,1H 
methoxyflurane 
C5-H6-O2 
2-Furyl methyl ether 
AR-1J4213 
CID117476 
ZINC02242715 
80407-56-3 
2-methoxy furan 
UNII-25Y8I1P35T 
OXCGHDNCMSOEBZ-UHFFFAOYSA-N 
25Y8I1P35T 
MFCD00003227 
Literature

Title: Structure and thermochemical properties of 2-methoxyfuran, 3-methoxyfuran, and their carbon-centered radicals using computational chemistry.

Journal: The journal of physical chemistry. A 20100805

Title: Structural studies on cycloadducts of furan, 2-methoxyfuran, and 5-trimethylsilylcyclopentadiene with maleic anhydride and N-methylmaleimide.

Journal: The Journal of organic chemistry 20080104

Title: Asymmetric Friedel-Crafts alkylation of methoxyfuran with nitroalkenes catalyzed by diphenylamine-tethered bis(oxazoline)-Zn(II) complexes.

Journal: Organic letters 20071108

Title: A 4-alkyl-substituted analogue of guaiacol shows greater repellency to savannah tsetse (Glossina spp.).

Journal: Journal of chemical ecology 20070501

Title: Cyclopropanation of enantiopure metal alkenyl carbenes with 2-methoxyfuran: a practical route to carboxycyclopropylglycine precursors.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

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