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119-64-2 | Naphthalene, 1,2,3,4-tetrahydro-
CAS No: 119-64-2 Catalog No: AG000OZZ MDL No:MFCD00001733
Product Description
Catalog Number:
AG000OZZ
Chemical Name:
Naphthalene, 1,2,3,4-tetrahydro-
CAS Number:
119-64-2
Molecular Formula:
C10H12
Molecular Weight:
132.2023
MDL Number:
MFCD00001733
IUPAC Name:
1,2,3,4-tetrahydronaphthalene
InChI:
InChI=1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2
InChI Key:
CXWXQJXEFPUFDZ-UHFFFAOYSA-N
SMILES:
C1CCc2c(C1)cccc2
UNII:
FT6XMI58YQ
NSC Number:
77451
RTECS Number:
QK3850000
UN Number:
1993
Properties
Complexity:
92.6
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
132.094g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
132.206g/mol
Monoisotopic Mass:
132.094g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.5
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| Identification and functional characterization of Sphingomonas macrogolitabida strain TFA genes involved in the first two steps of the tetralin catabolic pathway. | Journal of bacteriology 20030301 |
| Memory of chirality generated by spontaneous crystallization and asymmetric synthesis using the frozen chirality. | The Journal of organic chemistry 20030207 |
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| Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimer's disease. | Journal of medicinal chemistry 20021121 |
| An expedient enantioselective route to diaminotetralins: application in the preparation of analgesic compounds. | Organic letters 20021003 |
| Identification of a hydratase and a class II aldolase involved in biodegradation of the organic solvent tetralin. | Applied and environmental microbiology 20021001 |
| Highly enantioselective intra- and intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: host-guest interactions, product configuration, and the origin of the stereoselectivity in solution. | Journal of the American Chemical Society 20020710 |
| Metalloporphyrin-mediated asymmetric nitrogen-atom transfer to hydrocarbons: aziridination of alkenes and amidation of saturated C-H bonds catalyzed by chiral ruthenium and manganese porphyrins. | Chemistry (Weinheim an der Bergstrasse, Germany) 20020402 |
| Chiral capillary electrophoretic determination of the enantiomeric purity of tetrahydronaphthalenic derivatives, melatoninergic ligands, using highly sulfated beta-cyclodextrins. | Electrophoresis 20020401 |
| Aromatic as well as aliphatic hydrocarbon solvent axonopathy. | International journal of hygiene and environmental health 20020301 |
| Identical ring cleavage products during anaerobic degradation of naphthalene, 2-methylnaphthalene, and tetralin indicate a new metabolic pathway. | Applied and environmental microbiology 20020201 |
| Conformationally restrained analogues of sympathomimetic catecholamines. Synthesis and adrenergic activity of 5,6- and 6,7-dihydroxy-3,4-dihydrospiro[naphthalen-1(2H)-2',5'-morpholines]. | European journal of medicinal chemistry 20020101 |
| Vibrational study of polymorphism of tetralin derivative for treatment of cardiovascular diseases. | Biopolymers 20020101 |
| Antioxidative activity of hydroxylamines. ESR spectra of radicals derived from hydroxylamines. | Free radical research 20011201 |
| Synthesis of novel retinoid X receptor-selective retinoids. | The Journal of organic chemistry 20010824 |
| Direct observation of crystallization and aggregation in a phase-separating colloid-polymer suspension. | Physical review. E, Statistical, nonlinear, and soft matter physics 20010801 |
| Serotonin receptor and transporter ligands - current status. | Current medicinal chemistry 20010701 |
| Fused heterocyclic antioxidants: antioxidative activities of hydrocoumarins in a homogeneous solution. | Bioscience, biotechnology, and biochemistry 20010501 |
| Conversion of enediynes into quinones by antibody catalysis and in aqueous buffers: implications for an alternative enediyne therapeutic mechanism. | Journal of the American Chemical Society 20010418 |
| Direct separation of the stereoisomers of methoxytetrahydronaphthalene derivatives, new agonist and antagonist ligands for melatonin receptors, by liquid chromatography on cellulose chiral stationary phases. | Journal of chromatography. A 20010112 |
| Common solvent toxicity: autoxidation of respiratory redox-cyclers enforced by membrane derangement. | Zeitschrift fur Naturforschung. C, Journal of biosciences 20010101 |
| Carbon isotope fractionation in the decarboxylation of phenylpropiolic acid in hydrogen donating media. | Isotopes in environmental and health studies 20010101 |
| Effects of serotoninergic drugs on tremor induced by physostigmine in rats. | Behavioural brain research 20000501 |
| Tetralin as a substrate for camphor (cytochrome P450) 5-monooxygenase. | Archives of biochemistry and biophysics 19960815 |
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