tert-Butyl N-[4-(aminomethyl)phenyl]carbamate

Name: tert-Butyl N-[4-(aminomethyl)phenyl]carbamate
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CAS No. 220298-96-4
Cat. No. CS-W002926
Purity≥96%
MDL No.MFCD02183573

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tert-Butyl N-[4-(aminomethyl)phenyl]carbamate|CS-W002926

Structure of 220298-96-4

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General Information

CAS No. 220298-96-4
Cat. No. CS-W002926
Purity ≥96%
MDL No. MFCD02183573
Storage 4°C, protect from light, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₂H₁₈N₂O₂
Molecular Weight 222.29
Synonym(s) None
SMILES O=C(OC(C)(C)C)NC1=CC=C(C=C1)CN

Description

tert-Butyl N-[4-(aminomethyl)phenyl]carbamate features a benzylamine handle flanked by a robust tert-butyl carbamate protecting group, enabling selective deprotection under mild acidic conditions. This scaffold integrates seamlessly into peptide-based conjugates and bioorthogonal workflows, offering enhanced stability during synthesis and purification.

Application

tert-Butyl N-[4-(aminomethyl)phenyl]carbamate serves as a stable, bench-ready aminoalkyl building block for the synthesis of biologically relevant scaffolds. The protected amine enables orthogonal functionalization in multi-step sequences, while the arylmethyl handle facilitates direct coupling or derivatization. Its robust tert-butyl carbamate group resists premature deprotection under standard reaction conditions, simplifying purification and enhancing compatibility with diverse synthetic transformations.

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-H317
Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501

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Computational Chemistry Data

TPSA 64.35
LogP 2.4923
H_Acceptors 3
H_Donors 2
Rotatable_Bonds 2

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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tert-Butyl N-[4-(aminomethyl)phenyl]carbamate

CAS No. 220298-96-4

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