Cas no 87661-20-9 (Tert-butyl cyclopropanecarboxylate)

Tert-butyl cyclopropanecarboxylate structure
87661-20-9 structure
Product Name:Tert-butyl cyclopropanecarboxylate
CAS No:87661-20-9
MF:C8H14O2
MW:142.195562839508
MDL:MFCD09836696
CID:653853
Update Time:2024-10-26

Tert-butyl cyclopropanecarboxylate Chemical and Physical Properties

Names and Identifiers

    • tert-Butyl cyclopropanecarboxylate
    • Cyclopropanecarboxylic acid, 1,1-dimethylethyl ester
    • Cyclopropanecarboxylic acid tert-butyl ester
    • Boc-cyclopropane
    • t-butyl cyclopropanecarboxylate
    • tert-butyl cyclopropylcarboxylate
    • tert-ButylCyclopropanecarboxylate
    • FTEAAYMAQFBUJJ-UHFFFAOYSA-N
    • KM2538
    • TRA0094974
    • SY016843
    • V3856
    • ST24050084
    • 1,1-Dimethylethyl cyclopropanecarboxylate (ACI)
    • Tert-butyl cyclopropanecarboxylate
    • MDL: MFCD09836696
    • Inchi: 1S/C8H14O2/c1-8(2,3)10-7(9)6-4-5-6/h6H,4-5H2,1-3H3
    • InChI Key: FTEAAYMAQFBUJJ-UHFFFAOYSA-N
    • SMILES: O=C(C1CC1)OC(C)(C)C

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 140
  • Topological Polar Surface Area: 26.3

Experimental Properties

  • Boiling Point: 148.8±8.0℃ at 760 mmHg

Tert-butyl cyclopropanecarboxylate Pricemore >>

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Tert-butyl cyclopropanecarboxylate Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Potassium tert-butoxide Solvents: Tetrahydrofuran ;  20 min, -30 °C
1.2 Reagents: Ammonium chloride Solvents: Water
1.3 Solvents: Water
Reference
New reactions of γ-halo carbanions: simple synthesis of substituted tetrahydrofurans
Makosza, Mieczyslaw; et al, Chemistry - A European Journal, 2002, 8(18), 4234-4240

Production Method 2

Reaction Conditions
1.1 Reagents: Potassium tert-butoxide Solvents: Tetrahydrofuran ;  20 min, -30 °C
1.2 Reagents: Ammonium chloride Solvents: Water
1.3 Solvents: Water
Reference
New reactions of γ-halo carbanions: simple synthesis of substituted tetrahydrofurans
Makosza, Mieczyslaw; et al, Chemistry - A European Journal, 2002, 8(18), 4234-4240

Production Method 3

Reaction Conditions
1.1 Reagents: Potassium tert-butoxide Solvents: Tetrahydrofuran ;  20 min, -30 °C
1.2 Reagents: Ammonium chloride Solvents: Water
1.3 Solvents: Water
Reference
New reactions of γ-halo carbanions: simple synthesis of substituted tetrahydrofurans
Makosza, Mieczyslaw; et al, Chemistry - A European Journal, 2002, 8(18), 4234-4240

Production Method 4

Reaction Conditions
1.1 Reagents: Potassium tert-butoxide Solvents: Tetrahydrofuran ;  20 min, -30 °C
1.2 Reagents: Ammonium chloride Solvents: Water
1.3 Solvents: Water
Reference
New reactions of γ-halo carbanions: simple synthesis of substituted tetrahydrofurans
Makosza, Mieczyslaw; et al, Chemistry - A European Journal, 2002, 8(18), 4234-4240

Tert-butyl cyclopropanecarboxylate Raw materials

Tert-butyl cyclopropanecarboxylate Preparation Products

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