45778
1,2-二氢萘
analytical standard
别名:
Dialin
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关于此项目
经验公式（希尔记法）:
C10H10
化学文摘社编号:
分子量:
130.19
EC Number:
207-183-8
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1851372
MDL number:
InChI key
KEIFWROAQVVDBN-UHFFFAOYSA-N
InChI
1S/C10H10/c1-2-6-10-8-4-3-7-9(10)5-1/h1-3,5-7H,4,8H2
SMILES string
C1Cc2ccccc2C=C1
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.582 (lit.)
bp
89 °C/16 mmHg (lit.)
mp
−8 °C (lit.)
density
0.997 g/mL at 25 °C (lit.)
application(s)
environmental
format
neat
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General description
1,2-Dihydronaphthalene is a bicyclic hydrocarbon, which resembles naphthalene but shows partial unsaturation in one of its rings. Its derivatives find wide applications in natural compounds of therapeutic interest.
Application
1,2-Dihydronaphthalene may be used as an analytical standard for the determination of the analyte in polycyclic aromatic hydrocarbon (PAH) mixtures by gas chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
152.6 °F - closed cup
flash_point_c
67 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Retention indices for programmed-temperature capillary-column gas chromatography of polycyclic aromatic hydrocarbons
Lee ML, et al.
Analytical Chemistry, 51(6), 768-773 (1979)
Prediction of gas chromatographic retention indexes of polycyclic aromation compounds and nitrated polycyclic aromatic compounds
Rohrbaugh RH and Jurs PC
Analytical Chemistry, 58(6), 1210-1212 (1986)
The synthesis of novel dihydronaphthalenes and benzofluorenes
Novel Selenium-Mediated Rearrangements and Cyclisations, 77(6), 1210-1212 (2012)
Claudia Sanfilippo et al.
Biotechnology letters, 26(23), 1815-1819 (2005-01-27)
Chloroperoxidase from Caldariomyces fumago catalyses the oxidation of 1,2-dihydronaphthalene to (1R,2R)-(+)-dihydroxytetrahydronaphthalene in homogenous citrate buffer/ionic liquid mixtures, using t-butyl hydroperoxide as O2 donor. It tolerates up to 30 (v/v) 1,3-dimethylimidazolium methylsulfate or 1-butyl-3-methylimidazolium methylsulfate. The enzyme activity in these ionic
Márcia Kameyama et al.
Molecules (Basel, Switzerland), 16(11), 9421-9438 (2011-11-15)
A new approach for the synthesis of indatraline was developed using as the key step an iodine(III)-mediated ring contraction of a 1,2-dihydronaphthalene derivative. Behavioral tests were conducted to evaluate the effect of indatraline and of its precursor indanamide on the
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