tert-Butyl bis(2-aminoethyl)carbamate

Name: tert-Butyl bis(2-aminoethyl)carbamate
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CAS No. 556082-02-1
Cat. No. CS-0109852
Purity≥97%
MDL No.MFCD06797595

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tert-Butyl bis(2-aminoethyl)carbamate|CS-0109852

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General Information

CAS No. 556082-02-1
Cat. No. CS-0109852
Purity ≥97%
MDL No. MFCD06797595
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₉H₂₁N₃O₂
Molecular Weight 203.28
Synonym(s) 2-Methyl-2-propanyl bis(2-aminoethyl)carbamate
SMILES O=C(OC(C)(C)C)N(CCN)CCN

Description

tert-Butyl bis(2-aminoethyl)carbamate features a sterically hindered tert-butyl group paired with two pendant aminoethyl chains, enabling efficient protection of primary amines in peptide synthesis. This robust scaffold facilitates orthogonal functionalization and exhibits enhanced stability under standard reaction conditions.

Application

tert-Butyl bis(2-aminoethyl)carbamate serves as a versatile, bench-stable building block for the synthesis of amino-functionalized scaffolds. It enables efficient introduction of multiple amine handles in one step, facilitating rapid diversification in peptide mimetics and heterocyclic chemistry. The tert-butyl carbamate group offers orthogonal protection with mild acid-labile cleavage, while the primary amines support standard coupling reactions, making it ideal for iterative synthesis workflows requiring functional group tolerance and ease of purification.

Safety Information

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GHS Pictogram :	GHS No : GHS05
Signal Word : Danger	UN#: 1760
Class : 8	Packing Group : Ⅲ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

TPSA 81.58
LogP 0.1409
H_Acceptors 4
H_Donors 2
Rotatable_Bonds 4

Other Classifications

Building Blocks Functional Group Boc

Building Blocks Functional Group Amine

Key Words

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tert-Butyl bis(2-aminoethyl)carbamate

CAS No. 556082-02-1

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