Identification | More | [Name]
ETHYL 1,4-BENZODIOXAN-2-CARBOXYLATE | [CAS]
4739-94-0 | [Synonyms]
TIMTEC-BB SBB008613 Doxazosin Impurity 2 Doxazosin Impurity 16 2,3-Dihydro-2-Carboethoxy-1,4- ETHYL 1,4-BENZODIOXAN-2-CARBOXYLATE ETHYL 1,4-BENZODIOXANE-2-CARBOXYLATE Ethyl1,4-Benzodioxane-2-carboxylate> 2,3-Dihydro-2-carboethoxy-1, 4-benzodioxane 1,4-BENZODIOXAN-2-CARBOXYLIC ACID ETHYL ESTER 1,4-Benzodioxane-2-carboxylic Acid Ethyl Ester ETHYL 2,3-DIHYDRO-1,4-BENZODIOXIN-2-CARBOXYLATE Ethyl 2,3-dihydrobenzo[1,4]dioxine-2-carboxylate Ethyl 2,3-Dihydro-1,4-Benzodioxine-2-Carboxylate Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-2-carboxylate 2,3-DIHYDRO-BENZO[1,4]DIOXINE-2-CARBOXYLIC ACID ETHYL ESTER ethyl 3-(cyclohexa-1,3-dien-1-yl)-1,4-dioxine-2-carboxylate 1,4-Benzodioxin-2-carboxylic acid, 2,3-dihydro-, ethyl ester 2,3,4a,8a-tetrahydro-1,4-benzodioxin-3-carboxylic acid ethyl ester 1,4-Benzodioxan-2-carboxylic acid, ethyl ester, Ethyl 2,3-dihydro-1,4-benzodioxin-2-carboxylate | [Molecular Formula]
C11H12O4 | [MDL Number]
MFCD01099774 | [Molecular Weight]
208.21 | [MOL File]
4739-94-0.mol |
Chemical Properties | Back Directory | [Boiling point ]
88-95 °C/0.3 mmHg (lit.) | [density ]
1.208 g/mL at 25 °C
| [refractive index ]
n20/D 1.523
| [Fp ]
>230 °F
| [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
clear liquid | [color ]
Colorless to Yellow to Orange | [InChI]
InChI=1S/C11H12O4/c1-2-13-11(12)10-7-14-8-5-3-4-6-9(8)15-10/h3-6,10H,2,7H2,1H3 | [InChIKey]
DDIGEMWIKJMEIU-UHFFFAOYSA-N | [SMILES]
O1C2=CC=CC=C2OCC1C(OCC)=O | [CAS DataBase Reference]
4739-94-0(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed. | [WGK Germany ]
2
| [HazardClass ]
IRRITANT | [HS Code ]
2916399090 |
Hazard Information | Back Directory | [Uses]
2,3-Dihydro-1,4-benzodioxin-2-carboxylic Acid Ethyl Ester is an intermediate used to prepare presynaptic α2-adrenoreceptor antagonists and potential antidepressants. It is also used to prepare aminoalkylbenzodioxins as calcium antagonists. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 77, p. 5373, 1955 DOI: 10.1021/ja01625a050 |
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