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CS-W001157 4
Total: USD 88.00

Boc-C9-Br

  • CAS No. 1644575-06-3

  • Cat. No. CS-0199333
  • Purity≥97%
  • MDL No.MFCD31728409

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

Boc-C9-Br|CS-0199333

Structure of 1644575-06-3

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General Information

  • CAS No. 1644575-06-3
  • Cat. No. CS-0199333
  • Purity ≥97%
  • MDL No. MFCD31728409
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₇BrO₂
  • Molecular Weight 307.27
  • Synonym(s) None
  • SMILES O=C(OC(C)(C)C)CCCCCCCCCBr

Description

tert-Butyl 10-bromodecanoate features a brominated aliphatic chain terminating in a stable tert-butyl ester, enabling straightforward functionalization in late-stage modifications. This moisture-tolerant reagent facilitates efficient coupling reactions under standard conditions, offering reliable access to diverse alkylated derivatives.

Application

tert-Butyl 10-bromodecanoate serves as a versatile bromoester building block for late-stage functionalization in synthetic organic chemistry. The terminal bromide enables palladium-catalyzed cross-coupling reactions, while the tert-butyl ester provides stability and orthogonal deprotection under mild acidic conditions. Its linear aliphatic chain supports incorporation into complex molecular architectures, facilitating access to bioactive scaffolds and polymer intermediates with predictable reactivity and high bench stability.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   26.3
  • LogP   4.8438
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   9

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