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CS-W001157 4
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tert-Butyl (8-bromooctyl)carbamate

  • CAS No. 142356-35-2

  • Cat. No. CS-0043308
  • Purity≥95%
  • MDL No.MFCD24473139

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

tert-Butyl (8-bromooctyl)carbamate|CS-0043308

Structure of 142356-35-2

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General Information

  • CAS No. 142356-35-2
  • Cat. No. CS-0043308
  • Purity ≥95%
  • MDL No. MFCD24473139
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₂₆BrNO₂
  • Molecular Weight 308.26
  • Synonym(s) None
  • SMILES O=C(OC(C)(C)C)NCCCCCCCCBr

Description

tert-Butyl (8-bromooctyl)carbamate delivers a brominated alkyl chain tethered to a stable carbamate protecting group, enabling direct functionalization in late-stage synthesis. This bench-stable derivative facilitates efficient coupling reactions and selective transformations under standard conditions.

Application

tert-Butyl (8-bromooctyl)carbamate serves as a versatile protecting group for primary amines, enabling efficient synthesis of aminoalkyl building blocks. The bromide functionality facilitates subsequent palladium-catalyzed cross-coupling reactions, while the tert-butyl carbamate moiety offers excellent bench stability and ease of removal under mild acidic conditions. This compound functions reliably in multi-step synthetic sequences requiring orthogonal protection and functionalization.

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-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   38.33
  • LogP   4.2466
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   8

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