cis-Octahydroisoindole

98%

Reagent Code: #221423
label
Alias Miglinide intermediate 1; cis-hexahydroisoindoleline; cis-total hydrogen isoindole (miglinide); cis-total hydrogen isoindole; cis-total hydrogen isoindole; cis-total hydrogen isoindole hydrochloride; cis-total hydrogen isoindole
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CAS Number 1470-99-1

science Other reagents with same CAS 1470-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.21 g/mol
Formula C₈H₁₅N
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and central nervous system agents. Its rigid, fused ring structure and defined stereochemistry make it valuable for designing enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to influence potency, selectivity, and metabolic stability. Also utilized in asymmetric synthesis and catalysis as a scaffold for ligand design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿330.00
5g
10-20 days ฿1,060.00
100g
10-20 days ฿9,760.00
25g
10-20 days ฿3,080.00
cis-Octahydroisoindole
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Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and central nervous system agents. Its rigid, fused ring structure and defined stereochemistry make it valuable for designing enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to influence potency, selectivity, and metabolic stability. Also utilized in asymmetric synthesis and

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and central nervous system agents. Its rigid, fused ring structure and defined stereochemistry make it valuable for designing enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to influence potency, selectivity, and metabolic stability. Also utilized in asymmetric synthesis and catalysis as a scaffold for ligand design.

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