| Identification | More | [Name]
METHYL 1-CYCLOPENTENE-1-CARBOXYLATE | [CAS]
25662-28-6 | [Synonyms]
Methyl 1-cyclopentenoate
1-cyclopentene-1-carboxylate
1-(Methoxycarbonyl)cyclopentene
Methyl 1-cyclopentenecarboxylate
1-(carboxymethoxy)cyclopentadiene
Methyl cyclopent-1-enecarboxylate
METHYL CYCLOPENTENE-1-CARBOXYLATE
1-(Methoxycarbonyl)cyclopent-1-ene
METHYL 1-CYCLOPENTENE-1-CARBOXYLATE
Methyl cyclopent-1-ene-1-carboxylate
Methyl 1-cyclopentene-1-carboxylate 97%
1-Cyclopentenecarboxylic acid Methyl ester
CYCLOPENTENE-1-CARBOXYLIC ACID METHYL ESTER
1-CYCLOPENTENE-1-CARBOXYLIC ACID METHYL ESTER
Methyl 1-cyclopentene-1-carboxylate | [Molecular Formula]
C7H10O2 | [MDL Number]
MFCD00239506 | [Molecular Weight]
126.15 | [MOL File]
25662-28-6.mol |
| Chemical Properties | Back Directory | [Boiling point ]
76-78 °C/9 mmHg (lit.) | [density ]
1.031 g/mL at 20 °C(lit.)
| [refractive index ]
n20/D 1.4660(lit.)
| [Fp ]
135 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
Crystalline Powder or Low Melting Solid | [color ]
White to pale yellow | [BRN ]
2040162 | [InChIKey]
VTYCAXIAUKEGBQ-UHFFFAOYSA-N | [CAS DataBase Reference]
25662-28-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
10-23 | [HS Code ]
29162090 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless liquid | [Uses]
Methyl 1-cyclopentene-1-carboxylate may be used as starting material in the synthesis of pinnaic acid and halichlorine. It undergoes asymmetric oxidative Heck reaction with aryl boronic acids to form coupling products in the presence of chiral NHC (N-heterocyclic carbine)-palladium (II) complex. | [General Description]
Methyl 1-cyclopentene-1-carboxylate, a cyclic alkene, is a cyclopentene derivative. It participates in the synthesis of azulene derivatives by initially forming the corresponding cyclopropanol followed by oxy-Cope rearrangement. |
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