| 1-Chloromethyl naphthalene Basic information |
| Product Name: | 1-Chloromethyl naphthalene |
| Synonyms: | 1-(chloromethyl)-naphthalen;1-(Chloromethyl)naphthene;AKOS BBS-00004040;1-chloromethyl-naphthalen;1-Menaphthyl chloride;1-menaphthylchloride;1-(CHLOROMETHYL)NAPHTHALENE;1-CHLOROMETHYLNAPHTHYL |
| CAS: | 86-52-2 |
| MF: | C11H9Cl |
| MW: | 176.64 |
| EINECS: | 201-678-2 |
| Product Categories: | API Intermediate;Naphthalene series;Aryl;Building Blocks;C9 to C12;Chemical Synthesis;Naphthalene derivatives;API intermediates;Halogenated Hydrocarbons;Organic Building Blocks;bc0001 |
| Mol File: | 86-52-2.mol |
| 1-Chloromethyl naphthalene Chemical Properties |
| Melting point | 32 °C(lit.) |
| Boiling point | 291 °C |
| density | 1.18 g/mL at 25 °C(lit.) |
| refractive index | n |
| Fp | >230 °F |
| storage temp. | Keep in dark place,Sealed in dry,Room Temperature |
| form | Liquid After Melting |
| Specific Gravity | 1.18 |
| color | deep brown |
| Water Solubility | Insoluble in water. |
| Sensitive | Moisture Sensitive |
| BRN | 636885 |
| InChIKey | XMWGTKZEDLCVIG-UHFFFAOYSA-N |
| LogP | 3.97 at 20℃ |
| CAS DataBase Reference | 86-52-2(CAS DataBase Reference) |
| NIST Chemistry Reference | Naphthalene, 1-(chloromethyl)-(86-52-2) |
| EPA Substance Registry System | Naphthalene, 1-(chloromethyl)- (86-52-2) |
| Safety Information |
| Hazard Codes | C,Xn |
| Risk Statements | 21/22-34-36/37/38-36-20/21/22 |
| Safety Statements | 26-36/37/39-45-60-20-27 |
| RIDADR | UN 3261 8/PG 2 |
| WGK Germany | 3 |
| RTECS | QJ2800000 |
| TSCA | Yes |
| HazardClass | 8 |
| PackingGroup | III |
| HS Code | 29036990 |
| MSDS Information |
| Provider | Language |
|---|---|
| 1-Chloromethyl naphthalene | English |
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| 1-Chloromethyl naphthalene Usage And Synthesis |
| Chemical Properties | Solid |
| Uses | 1-(Chloromethyl)naphthalene is a key material for synthesis dye pigment and as fluorescent brightening agent. It is employed in synthetic resin and medicine. Palladium-catalyzed nucleophilic dearomatization of chloromethyl naphthalene derivatives produce ortho- or para-substituted carbocycles in satisfactory to excellent yields. |
| General Description | Kinetics and dissociation mechanism of 1-(chloromethyl)naphthalene following 266nm photoexcitation has been studied. Intermolecular nucleophilic dearomatization of 1-chloromethyl naphthalene with various activated methylene compounds has been investigated. |
| 1-Chloromethyl naphthalene Preparation Products And Raw materials |
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