Fmoc-(R)-1,2,3,4-Tetrahydro-isoquinoline-3-aceticacid

Name: Fmoc-(R)-1,2,3,4-Tetrahydro-isoquinoline-3-aceticacid
Brand: ChemScene
Availability: InStock
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CAS No. 332064-67-2
Cat. No. CS-0060608
Purity≥98%
MDL No.None

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

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Fmoc-(R)-1,2,3,4-Tetrahydro-isoquinoline-3-aceticacid|CS-0060608

Structure of 332064-67-2

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General Information

CAS No. 332064-67-2
Cat. No. CS-0060608
Purity ≥98%
MDL No. None
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₂₆H₂₃NO₄
Molecular Weight 413.47
Synonym(s) Fmoc-(R)-2-tetrahydroisoquinoline acetic acid
SMILES C1=CC=C2CN([C@H](CC2=C1)CC(=O)O)C(=O)OCC3C4=CC=CC=C4C5=CC=CC=C53

Description

Fmoc-(R)-1,2,3,4-Tetrahydro-isoquinoline-3-acetic acid serves as a chiral building block for peptide synthesis, featuring a rigid, electron-rich tetrahydroisoquinoline scaffold. The Fmoc group enables efficient N-terminal protection, while the acetic acid side chain facilitates conjugation and structural diversity in bioactive peptide libraries.

Application

Fmoc-(R)-1,2,3,4-Tetrahydro-isoquinoline-3-acetic acid serves as a versatile building block for the synthesis of peptidomimetics and bioactive heterocycles. The Fmoc group enables efficient solid-phase peptide synthesis, while the tetrahydroisoquinoline core provides structural rigidity and favorable pharmacophoric properties. It exhibits excellent bench stability, compatibility with standard coupling conditions, and facilitates orthogonal functionalization in multi-step syntheses.

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-H312-H332
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501

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Computational Chemistry Data

TPSA 66.84
LogP 4.8371
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 4

Other Classifications

Building Blocks Functional Group Carboxylic Acid

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Aromatic heterocycle compounds Tetrahydroisoquinoline compounds

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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Fmoc-(R)-1,2,3,4-Tetrahydro-isoquinoline-3-aceticacid

CAS No. 332064-67-2

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