Β-溴乙氧基苯
beta-Bromophenetole
CAS: 589-10-6
Molecular Formula: C8H9BrO
Β-溴乙氧基苯 - Names and Identifiers
| Name | beta-Bromophenetole |
| Synonyms | -Bromophenetole β-Bromophenetole PHENOXYETHYLBROMIDE beta-Bromophenetole 2-Phenoxyethylbromide (2-BROMETHOXY)BENZENE (2-bromoethoxy)benzene Phenetole, beta-bromo- (2-bromoethoxy)-benzen (3-bromopropyl)benzene (2-BROMOETHOXY)BENZENE Benzene,(2-bromoethoxy)- Benzene, (2-bromoethoxy)- 2-Bromoethyl phenyl ether 2-BROMOETHYL PHENYL ETHER beta-Bromoethyl phenyl ether |
| CAS | 589-10-6 |
| EINECS | 209-634-4 |
| InChI | InChI=1/C9H11Br/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2 |
Β-溴乙氧基苯 - Physico-chemical Properties
| Molecular Formula | C8H9BrO |
| Molar Mass | 201.06 |
| Density | 1.45 |
| Melting Point | 31-34°C(lit.) |
| Boling Point | 144°C40mm Hg(lit.) |
| Flash Point | 150°F |
| Water Solubility | Insoluble in water. |
| Solubility | Solubility in methanol is almost transparent. Soluble in chloroform and ethyl acetate. |
| Vapor Presure | 0.17mmHg at 25°C |
| Appearance | Liquid After Melting |
| Color | Clear colorless |
| BRN | 508290 |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.555-1.557 |
| Physical and Chemical Properties | Melting point 39 ° C, boiling point 240-250 ° C (decomposition),114-117 ° C (1.33kPa). |
| Use | For the synthesis of nefazodone, phenoxymepidone and other raw materials |
Β-溴乙氧基苯 - Risk and Safety
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R22 - Harmful if swallowed |
| Safety Description | S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| UN IDs | 1325 |
| WGK Germany | 3 |
| TSCA | Yes |
| HS Code | 29093038 |
| Hazard Note | Irritant |
| Hazard Class | 4.1 |
| Packing Group | II |
Β-溴乙氧基苯 - Reference Information
| NIST chemical information | Information provided by: webbook.nist.gov (external link) |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| use | pharmaceutical intermediates. for the synthesis of naphthalazodone, phenoxypimidone and other raw materials |
| Production method | is obtained by the reaction of phenol and dibromoethane. Phenol, dibromoethane and sodium hydroxide are stirred and mixed in a reaction pot, reacted at 110 ℃ for 6 hours, dibromoethane is recovered, the recovery amount is about 60%, washed with 5% sodium hydroxide solution and water, the oil layer is divided, distilled under reduced pressure, and the fraction 130-150 ℃(6.7kPa) is collected to obtain (2-bromoethoxy) benzene. |
Last Update：2024-04-09 19:05:09
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View History
Β-溴乙氧基苯
3-(4-氟-1-氧代异吲哚啉-2-基)哌啶-2,6-二酮
1,2-Cyclohexanediol, 1-(aminomethyl)-, (1R,2R)-rel- (9CI)
2H-1-Benzopyran-2-one, 4-hydroxy-7,8-dimethoxy-
CITROTONE B
Einecs 235-002-2
5-hydroxy-2-methoxypridine
5-甲基-吡咯-2-甲酸乙酯
1,2-Propanediol, 3-[(4-methylphenyl)thio]-
Levonorgestrel EP IMP M
3-(4-氟-1-氧代异吲哚啉-2-基)哌啶-2,6-二酮
1,2-Cyclohexanediol, 1-(aminomethyl)-, (1R,2R)-rel- (9CI)
2H-1-Benzopyran-2-one, 4-hydroxy-7,8-dimethoxy-
CITROTONE B
Einecs 235-002-2
5-hydroxy-2-methoxypridine
5-甲基-吡咯-2-甲酸乙酯
1,2-Propanediol, 3-[(4-methylphenyl)thio]-
Levonorgestrel EP IMP M