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CS-W001157 4
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tert-Butyl 2-(bromomethyl)prop-2-enoate,98% (stabilized with MEHQ)

  • CAS No. 53913-96-5

  • Cat. No. CS-0651179
  • Purity95% (stabilized with MEHQ)
  • MDL No.None

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

tert-Butyl 2-(bromomethyl)prop-2-enoate,98% (stabilized with MEHQ)|CS-0651179

Structure of 53913-96-5

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General Information

  • CAS No. 53913-96-5
  • Cat. No. CS-0651179
  • Purity 95% (stabilized with MEHQ)
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₁₃BrO₂
  • Molecular Weight 221.09
  • Synonym(s) None
  • SMILES O=C(C(CBr)=C)OC(C)(C)C

Description

tert-Butyl 2-(bromomethyl)prop-2-enoate, 98% (stabilized with MEHQ) features a reactive bromomethyl group conjugated to an enoate moiety, enabling efficient coupling in synthetic transformations. The tert-butyl ester provides stability and ease of handling, while MEHQ prevents radical-induced decomposition. This bench-stable reagent integrates readily into diverse reaction sequences requiring electrophilic alkylating agents.

Application

tert-Butyl 2-(bromomethyl)prop-2-enoate serves as a versatile vinyl-bearing bromide synthon, enabling efficient Michael additions and palladium-catalyzed cross-couplings. The stabilized formulation ensures bench longevity and minimizes decomposition during storage. Its terminal alkene functionality facilitates further derivatization in heterocycle synthesis and late-stage functionalization workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3265
Class : 8
Packing Group : Ⅱ
Hazard Statements : H302-H314
Precautionary Statements : P264-P270-P271-P280-P304+P340-P330-P331-P363-P501

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Computational Chemistry Data

  • TPSA   N/A
  • LogP   N/A
  • H_Acceptors   N/A
  • H_Donors   N/A
  • Rotatable_Bonds   N/A

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