1075727-06-8 | 2-(2-carboxyethyl)-1-[(3,4-dimethoxyphenyl)methyl]-,1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-isoquinolinium benzenesulfonate

Packsize	Purity	Availability	Price	Discounted Price
25mg		1 week	$1,669.00	$1,168.00

Description

• Catalog Number: AE21648
• Chemical Name: 2-(2-carboxyethyl)-1-[(3,4-dimethoxyphenyl)methyl]-,1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-isoquinolinium benzenesulfonate
• CAS Number: 1075727-06-8
• Molecular Formula: C30H37NO9S
• Molecular Weight: 587.6811
• MDL Number: MFCD20526437
• SMILES: [O-]S(=O)(=O)c1ccccc1.COc1cc(ccc1OC)C[C@@H]1c2cc(OC)c(cc2CC[N@+]1(C)CCC(=O)O)OC

Upstream Synthesis Route

The compound (1R,2R)-2-(2-Carboxyethyl)-1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium benzenesulfonate is a versatile reagent that finds extensive application in chemical synthesis. It serves as a key intermediate in the production of various organic compounds, particularly in the synthesis of complex molecules with pharmaceutical or biological significance.One notable use of this compound in chemical synthesis is as a chiral building block. The presence of both a tetrahydroisoquinoline and a carboxyethyl group in its structure provides opportunities for stereochemical control in synthetic pathways. By utilizing the chiral centers present in the molecule, chemists can access enantiomerically pure products, which is crucial in the development of pharmaceuticals and agrochemicals where the stereochemistry significantly impacts the biological activity.Furthermore, the benzenesulfonate moiety in the compound serves as a protecting group for the tetrahydroisoquinoline ring, allowing selective functionalization of other reactive sites in the molecule. This protection-deprotection strategy enhances the synthetic efficiency and enables the construction of complex molecular architectures with precision.Overall, the (1R,2R)-2-(2-Carboxyethyl)-1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium benzenesulfonate is a valuable tool in chemical synthesis, enabling chemists to access a wide range of structurally diverse compounds with controlled stereochemistry and functional group tolerance.