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Home Other Building Blocks 1(2H)-Naphthalenone, 3,4-dihydro-4-hydroxy-

1(2H)-Naphthalenone, 3,4-dihydro-4-hydroxy-

CAS No.:
21032-12-2
Catalog Number:
AG002KPH
Molecular Formula:
C10H10O2
Molecular Weight:
162.1852
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Product Description
Catalog Number:
AG002KPH
Chemical Name:
1(2H)-Naphthalenone, 3,4-dihydro-4-hydroxy-
CAS Number:
21032-12-2
Molecular Formula:
C10H10O2
Molecular Weight:
162.1852
MDL Number:
MFCD11036279
IUPAC Name:
4-hydroxy-3,4-dihydro-2H-naphthalen-1-one
InChI:
InChI=1S/C10H10O2/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-4,9,11H,5-6H2
InChI Key:
BGPJTIXJFAGUIF-UHFFFAOYSA-N
SMILES:
O=C1CCC(c2c1cccc2)O
Properties
Complexity:
188  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
162.068g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
162.188g/mol
Monoisotopic Mass:
162.068g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.9  
Literature
Title Journal
Antihyperglycemic agents from Ammannia multiflora. Natural product communications 20120701
Bioenhancing and antimycobacterial agents from Ammannia multiflora. Planta medica 20120101
Characterization of indigenous Rhodococcus sp. 602, a strain able to accumulate triacylglycerides from naphthyl compounds under nitrogen-starved conditions. Research in microbiology 20100401
Diastereoselective synthesis of 4-hydroxytetralones via a cascade Stetter-aldol reaction catalyzed by N-heterocyclic carbenes. The Journal of organic chemistry 20100101
Antitubercular constituents from the roots of Engelhardia roxburghiana. Planta medica 20050201
Properties