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CS-W001157 4
Total: USD 88.00

(Bromomethyl)cyclopentane

  • CAS No. 3814-30-0

  • Cat. No. CS-W004985
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

(Bromomethyl)cyclopentane|CS-W004985

Structure of 3814-30-0

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General Information

  • CAS No. 3814-30-0
  • Cat. No. CS-W004985
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₁₁Br
  • Molecular Weight 163.06
  • Synonym(s) Cyclopentylmethyl Bromide
  • SMILES BrCC1CCCC1

Description

Bromomethylcyclopentane features a reactive bromomethyl group attached to a cyclopentane ring, enabling efficient functionalization in synthetic transformations. This bench-stable alkylating agent integrates readily into C–C bond-forming processes and serves as a key intermediate in the construction of complex cyclic architectures.

Synthesis

  • Route1

    References

    • Samsel, E. G.; Kochi, J. K. Journal of the American Chemical Society, 1986 , vol. 108, # 16 p. 4790 - 4804
  • Route2
    • Cyclopentylmethyl 4-methylbenzene-1-sulfonate|CS-0217934
      21856-53-1
    • ~98%
    • In-stock
      (Bromomethyl)cyclopentane|CS-W004985
      3814-30-0

    References

    • ANADYS PHARMACEUTICALS, INC. Patent: WO2008/82725 A1, 2008 ; Location in patent: Page/Page column 69-70 ;
  • Route3
    • Cyclopentylmethyl methanesulfonate|CS-0969357
      73017-76-2
    • ~%
    • In-stock
      (Bromomethyl)cyclopentane|CS-W004985
      3814-30-0

    References

    • NOVARTIS AG; NOVARTIS PHARMA GmbH; VICURON PHARMACEUTICALS, INC Patent: WO2006/127576 A2, 2006 ; Location in patent: Page/Page column 25 ; WO 2006/127576 A2

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS02,GHS07
Signal Word : Danger
UN#: 1993
Class : 3
Packing Group : Ⅲ
Hazard Statements : H226-H302-H315-H319-H335
Precautionary Statements : P210-P261-P280-P301+P330+P331-P302+P352-P304+P340

Quality Control

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Computational Chemistry Data

  • TPSA   0
  • LogP   2.5715
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   1

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