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CS-W001157 4
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tert-Butyl (10-bromodecyl)carbamate

  • CAS No. 887353-29-9

  • Cat. No. CS-0119811
  • Purity≥97%
  • MDL No.MFCD03788821

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

tert-Butyl (10-bromodecyl)carbamate|CS-0119811

Structure of 887353-29-9

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General Information

  • CAS No. 887353-29-9
  • Cat. No. CS-0119811
  • Purity ≥97%
  • MDL No. MFCD03788821
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₃₀BrNO₂
  • Molecular Weight 336.31
  • Synonym(s) None
  • SMILES O=C(OC(C)(C)C)NCCCCCCCCCCBr

Description

tert-Butyl (10-bromodecyl)carbamate features a brominated alkyl chain flanked by a stable tert-butyl carbamate protecting group. This bifunctional scaffold enables direct incorporation into polymer backbones or conjugation workflows, where the terminal bromide serves as a reactive handle for cross-coupling reactions under standard conditions. The robust protection remains intact during synthetic manipulations, facilitating efficient access to functionalized materials.

Application

tert-Butyl (10-bromodecyl)carbamate serves as a stable, bench-ready protecting group for primary amines, enabling straightforward installation and orthogonal removal under mild acidic conditions. The bromide functionality facilitates downstream functionalization via palladium-catalyzed cross-coupling reactions, making it a versatile building block for the synthesis of complex aliphatic amines and functionalized heterocycles in medicinal chemistry and materials science.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05,GHS09
Signal Word : Danger
UN#: 3077
Class : 9
Packing Group : Ⅲ
Hazard Statements : H318-H411
Precautionary Statements : P273-P280-P391-P501

Quality Control

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Computational Chemistry Data

  • TPSA   38.33
  • LogP   5.0268
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   10

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