Cas no 36865-40-4 (1-bromo-3-ethoxypropane)

1-bromo-3-ethoxypropane structure
1-bromo-3-ethoxypropane structure
Product Name:1-bromo-3-ethoxypropane
CAS No:36865-40-4
MF:C5H11BrO
MW:167.044241189957
MDL:MFCD07780182
CID:315111
PubChem ID:260493
Update Time:2025-04-19

1-bromo-3-ethoxypropane Chemical and Physical Properties

Names and Identifiers

    • Propane,1-bromo-3-ethoxy-
    • 3-ethoxypropyl bromide
    • 1-bromo-3-ethoxypropane
    • Propane, 1-bromo-3-ethoxy-
    • 1-bromo-3-ethoxy-propane
    • 3-ETHOXYPROPYLBROMIDE
    • SCHEMBL1074128
    • 36865-40-4
    • MFCD07780182
    • NSC-91822
    • NCIOpen2_001416
    • AKOS009291875
    • CS-0217812
    • FT-0695248
    • NSC91822
    • 3-ethoxy-1-bromopropane
    • EN300-86016
    • 3-bromopropyl ethyl ether
    • DTXSID80293736
    • MDL: MFCD07780182
    • Inchi: 1S/C5H11BrO/c1-2-7-5-3-4-6/h2-5H2,1H3
    • InChI Key: JOZWPJGRGUOZGY-UHFFFAOYSA-N
    • SMILES: BrCCCOCC

Computed Properties

  • Exact Mass: 165.99933
  • Monoisotopic Mass: 165.999
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 7
  • Rotatable Bond Count: 4
  • Complexity: 31.3
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 9.2A^2
  • XLogP3: 1.6

Experimental Properties

  • Density: 1.278
  • Boiling Point: 129.7°Cat760mmHg
  • Flash Point: 44.3°C
  • Refractive Index: 1.443
  • PSA: 9.23

1-bromo-3-ethoxypropane Pricemore >>

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1-bromo-3-ethoxypropane Related Literature

  • 1. 638. The constitution of yohimbine and related alkaloids. Part XIII. The synthesis of some 12H-indolo[2,3-a]pyridocolinium salts substituted at the 2-position
    G. A. Swan,P. R. Thomas J. Chem. Soc. 1963 3440
  • D. W. Cameron,E. M. Hildyard J. Chem. Soc. C 1968 166
  • 3. Notes
    D. W. McBride,S. L. Stafford,F. G. A. Stone,Denys M. Heinekey,Ian T. Millar,Frederick G. Mann,Arthur Finch,P. J. Gardner,J. C. Lockhart,Asharam Bhati,J. M. Z. Gladych,R. N. Brown,G. Winter,S. K. Tobia,N. E. Milad,G. E. Ficken,D. J. Fry,D. C. Nonhebel,Lanson S. El-Assal,Samiha M. A. El-Wahhab,Nargues S. Baceili,P. T. Armitage,C. M. French,L. J. Haynes,J. R. Plimmer,W. M. Sue-Ho,C. E. Seaforth,Barbara A. Grzybowska,J. H. Knox,A. F. Trotman-Dickenson,R. J. Abraham,L. D. Hall,L. Hough,K. A. McLauchlan,H. J. Miller,H. R. Arthur,Rosalind P. K. Chan,A. Fischer,D. I. Stedman,J. Vaughan,A. R. Katritzky,R. E. Reavill,H. C. Beyerman,G. J. Heiszwolf,M. H. B. Stiddard,C. J. W. Brooks,W. L. Stafford,C. D. Baker,F. D. Gunstone J. Chem. Soc. 1963 723
  • 4. 871. Colouring matters of the aphididae. Part XXIII. Synthesis of the xanthoaphin chromophore
    D. W. Cameron,R. I. T. Cromartie,D. G. I. Kingston,G. B. V. Subramanian J. Chem. Soc. 1964 4565
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