Cas no 17860-87-6 (L-Ascorbic acid,2-O-methyl-)
L-Ascorbic acid,2-O-methyl- structure
Product Name:L-Ascorbic acid,2-O-methyl-
CAS No:17860-87-6
MF:C7H10O6
MW:190.150702953339
CID:190130
PubChem ID:54726398
Update Time:2025-04-19
L-Ascorbic acid,2-O-methyl- Chemical and Physical Properties
Names and Identifiers
-
- L-Ascorbic acid,2-O-methyl-
- 2-(1,2-dihydroxyethyl)-3-hydroxy-4-methoxy-2H-furan-5-one
- 2-O-methylascorbic acid
- 2-Methylascorbic acid
- 2-o-methylhex-1-enofuranos-3-ulose
- AC1L414Z
- AC1Q6D78
- AR-1E4535
- NSC219890
- ASCORBIC ACID, 2-O-METHYL-
- 17860-87-6
- NSC-219890
- UNII-OE7EI0514F
- 2-METHYL-L-ASCORBIC ACID
- 2-O-Methyl-L-ascorbic acid
- OE7EI0514F
- Q27896126
- 2-O-METHYLASCORBIC ACID, (+)-
- L-Ascorbic acid, 2-O-methyl-
- CHEMBL452673
- SCHEMBL3307566
- NSC 219890
-
- Inchi： 1S/C7H10O6/c1-12-6-4(10)5(3(9)2-8)13-7(6)11/h3,5,8-10H,2H2,1H3/t3-,5+/m0/s1
- InChI Key： JBXPKMHATRSERD-WVZVXSGGSA-N
- SMILES： O1C(C(=C([C@H]1[C@H](CO)O)O)OC)=O
Computed Properties
- Exact Mass: 190.0477
- Monoisotopic Mass: 190.047738
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 13
- Rotatable Bond Count: 3
- Complexity: 245
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 2
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: _1.5
- Topological Polar Surface Area: 96.2
Experimental Properties
- Density: 1.55
- Boiling Point: 433.1°Cat760mmHg
- Flash Point: 183.2°C
- Refractive Index: 1.566
- PSA: 96.22
- LogP: -1.31900
L-Ascorbic acid,2-O-methyl- Related Literature
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P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. Buda Phys. Chem. Chem. Phys., 2011,13, 10270-10279
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Christian K. Rank,Alexander W. Jones,Tatjana Wall,Patrick Di Martino-Fumo,Sarah Schr?ck,Markus Gerhards,Frederic W. Patureau Chem. Commun., 2019,55, 13749-13752
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3. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
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