4721-98-6 | 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$69.00	$48.00
250mg	97%	in stock	$90.00	$63.00
1g	97%	in stock	$230.00	$161.00
5g	97%	in stock	$667.00	$467.00
10g	97%	in stock	$1,070.00	$749.00
25g	97%	in stock	$2,004.00	$1,403.00

Description

• Catalog Number: AG16632
• Chemical Name: 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline
• CAS Number: 4721-98-6
• Molecular Formula: C12H15NO2
• Molecular Weight: 205.253
• MDL Number: MFCD01694515
• SMILES: COc1cc2C(=NCCc2cc1OC)C
• NSC Number: 144726

Computed Properties

• Complexity: 252
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• XLogP3: 1.6

Upstream Synthesis Route

6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline serves as a valuable building block in chemical synthesis due to its unique structural features and versatile reactivity. This compound has found wide application in the synthesis of various biologically active molecules, pharmaceuticals, and natural products. Its substituted isoquinoline core provides a diverse array of functional groups for further modification, allowing chemists to tailor its properties for specific applications. By incorporating 6,7-dimethoxy-1-methyl-3,4-dihydroisoquinoline into synthetic routes, researchers can access complex molecular frameworks with high efficiency and control, making it a valuable tool in modern organic chemistry.

Literature

• Synthesis and structure-activity relationship of disubstituted benzamides as a novel class of antimalarial agents.

  Bioorganic & medicinal chemistry letters 20120715

• Opportunities offered by chiral η⁶-arene/N-arylsulfonyl-diamine-RuII catalysts in the asymmetric transfer hydrogenation of ketones and imines.

  Molecules (Basel, Switzerland) 20110628

• Novel 5, 6-Dihydropyrrolo[2,1-a]isoquinolines as Scaffolds for Synthesis of Lamellarin Analogues.

  Evidence-based complementary and alternative medicine : eCAM 20110101

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• An expedient route to 2,3-substituted and fused benzo[a]quinolizine-4-thione framework via ring annulation with beta-oxodithioesters.

  Organic letters 20010125