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tert-Butyl (6-bromobenzo[d]thiazol-2-yl)carbamate

  • CAS No. 1244041-71-1

  • Cat. No. CS-0132547
  • Purity≥95%
  • MDL No.MFCD16036619

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

tert-Butyl (6-bromobenzo[d]thiazol-2-yl)carbamate|CS-0132547

Structure of 1244041-71-1

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General Information

  • CAS No. 1244041-71-1
  • Cat. No. CS-0132547
  • Purity ≥95%
  • MDL No. MFCD16036619
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₃BrN₂O₂S
  • Molecular Weight 329.21
  • Synonym(s) tert-butyl 6-bromobenzo[d]thiazol-2-ylcarbamate
  • SMILES O=C(OC(C)(C)C)NC1=NC2=CC=C(Br)C=C2S1

Description

tert-Butyl (6-bromobenzo[d]thiazol-2-yl)carbamate serves as a stable, bench-ready building block for constructing brominated heterocyclic scaffolds. The carbamate moiety enables direct incorporation into peptide or small-molecule frameworks, while the 6-bromo substitution facilitates subsequent cross-coupling reactions under standard conditions.

Application

tert-Butyl (6-bromobenzo[d]thiazol-2-yl)carbamate serves as a versatile building block for the synthesis of brominated benzo[d]thiazole scaffolds. The protected amine enables orthogonal functionalization in late-stage diversification, while the bromine substituent facilitates palladium-catalyzed cross-coupling reactions. Bench-stable and readily purified by column chromatography, it functions effectively in iterative heterocycle construction and medicinal chemistry campaigns requiring precise substitution patterns.

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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

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Computational Chemistry Data

  • TPSA   51.22
  • LogP   4.4058
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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