ChemicalBook > Product Catalog > Chemical Reagents > Organic reagents > The polycyclic compound > 1,2-DIHYDRONAPHTHALENE
1,2-DIHYDRONAPHTHALENE
1,2-DIHYDRONAPHTHALENE Basic information
- Product Name:
- 1,2-DIHYDRONAPHTHALENE
- Synonyms:
-
- DELTA1-DIALIN
- 1,2-DIHYDRONAPHTHALENE
- 1,2-Dialin
- 1,2-dihydro-naphthalen
- Dialin
- Diolin
- Dihydronaphthalene
- 1,2-DIHYDRONAPHTHALENE OEKANAL, 250 MG
- CAS:
- 447-53-0
- MF:
- C10H10
- MW:
- 130.19
- EINECS:
- 207-183-8
- Product Categories:
-
- Building Blocks
- Chemical Synthesis
- Alpha Sort
- Analytical Standards
- AromaticsVolatiles/ Semivolatiles
- Organic Building Blocks
- Chemical Class
- D
- DAlphabetic
- DID - DINAnalytical Standards
- Hydrocarbons
- NaphthalenesChemical Class
- NeatsAnalytical Standards
- PAHsMore...Close...
- Arenes
- Building Blocks
- Organic Building Blocks
- Mol File:
- 447-53-0.mol
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1,2-DIHYDRONAPHTHALENE Chemical Properties
- Melting point:
- −8 °C(lit.)
- Boiling point:
- 89 °C16 mm Hg(lit.)
- Density
- 0.997 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.582(lit.)
- Flash point:
- 153 °F
- storage temp.
- Sealed in dry,Room Temperature
- color
- Colorless to Light yellow
- Water Solubility
- Not miscible or difficult to mix with water.
- BRN
- 1851372
- CAS DataBase Reference
- 447-53-0(CAS DataBase Reference)
- EPA Substance Registry System
- Naphthalene, 1,2-dihydro- (447-53-0)
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Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- RTECS
- QJ4375000
- HS Code
- 29029000
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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1,2-DIHYDRONAPHTHALENE Usage And Synthesis
Chemical Properties
CLEAR LIGHT YELLOW TO SLIGHTLY BROWN LIQUID
Definition
ChEBI: A dihydronaphthalene hydrogenated at C-1 and C-2.
Synthesis Reference(s)
Tetrahedron Letters, 28, p. 2481, 1987 DOI: 10.1016/S0040-4039(00)95446-7
Synthesis
Dissolve 1,2-naphthoquinone (0.18 mmol) in ethanol (3 mL). NaBH4 (73 mg, 1.93 mmol) suspended in ethanol (3 mL) was added dropwise to the reaction mixture. The mixture was stirred at room temperature under nitrogen. After 1.5 hours, the mixture was poured into ice water (50 mL). Acidify the mixture with HCl (0.5 M). The mixture was extracted with CH2Cl2. The mixture was dried over magnesium sulfate. The mixture was concentrated to give 1,2-dihydroxynaphthalene.
1,2-DIHYDRONAPHTHALENESupplier
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
- Tel
- 021-61259108 18621169109
- market03@meryer.com
Alfa Aesar
- Tel
- 400-6106006
- saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
Syntechem Co.,Ltd
- Tel
- info@syntechem.com
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