China (Mainland)
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2,7-Dihydroxynaphthalene CAS NO.582-17-2
- Min.Order: 1 Kilogram
- Payment Terms: L/C,D/A,D/P,T/T,Other
- Product Details
Keywords
- 2,7-Dihydroxynaphthalene
- 582-17-2
- 2,7-Dihydroxynaphthalene
Quick Details
- ProName: 2,7-Dihydroxynaphthalene
- CasNo: 582-17-2
- Molecular Formula: C10H8O2
- Appearance: Light yellow to grey needle crystal
- Application: For Organic synthsis
- DeliveryTime: PROMPT
- PackAge: IN 25kg drums
- Port: SHANGHAI
- ProductionCapacity: 10 Metric Ton/Month
- Purity: 98.0% Min
- Storage: Room temperature
- Transportation: As Per MSDS
- LimitNum: 1 Kilogram
- Heavy metal: N/A
- Grade: Industrial Grade,Food Grade,Pharma Gra...
- Transporttation: N/A
Superiority
| 2,7-Dihydroxynaphthalene Basic information |
| Product Name: | 2,7-Dihydroxynaphthalene |
| Synonyms: | C.I. 76645;c.i.76645;CI 76645;Naphthalene-2,7-Diol;Naphthalenediol-(2,7);naphthalenediol-2,7;2,7-DIHYDROXYNAPTHALENE;2,7-DIHYDROXYNAPHTHALENE |
| CAS: | 582-17-2 |
| MF: | C10H8O2 |
| MW: | 160.17 |
| EINECS: | 209-478-7 |
| Product Categories: | FINE Chemical & INTERMEDIATES;Aromatics;API intermediates;Building Blocks;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Polyols |
| Mol File: | 582-17-2.mol |
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Details
| 2,7-Dihydroxynaphthalene Chemical Properties |
| mp | 185-190 °C(lit.) |
| Water Solubility | insoluble |
| BRN | 2042383 |
| CAS DataBase Reference | 582-17-2(CAS DataBase Reference) |
| NIST Chemistry Reference | 2,7-Naphthalenediol(582-17-2) |
| EPA Substance Registry System | 2,7-Naphthalenediol(582-17-2) |
| Safety Information |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36-37/39 |
| WGK Germany | 2 |
| RTECS | QJ4780000 |
| HS Code | 29072900 |
| 2,7-Dihydroxynaphthalene Usage And Synthesis |
| Chemical Properties | Light yellow to grey needle crystal |
| Usage | Starting material for the synthesis of sulfonic acids1 and divinylnaphthalenes.2 |
| Usage | 2,7-Naphthalenediol is a reagent used in the preparation of monomers of high carbon materials. Also used in the synthesis of splitomicin analogues. |