525-72-4

Basic information

• Product Name: 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol
• Synonyms: (R)-Salsolinol;1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol;Isoquinoline, 1,2,3,4-tetrahydro-6,7-dihydroxy-1-methyl-;[R,(+)]-1-Methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol;1,2,3,4-Tetrahydro-6,7-dihydroxy-1-methylisoquinoline;1-Methyl-1,2,3,4-tetrahydro-6,7-isoquinolinediol;Sasolinol;1-Methyl-6,7-dihydroxytetrahydroisoquinoline
• CAS NO: 525-72-4
• Molecular Formula: C₁₀H₁₃NO₂
• Molecular Weight: 179.22
• Mol File: 525-72-4.mol
• Article Data: 10

Chemical Properties

• Melting Point: 181-183 °C
• Boiling Point: 362.6°Cat760mmHg
• Flash Point: 175.4°C
• Appearance: /
• Density: 1.201
• PKA: 9.15±0.40(Predicted)
• CAS DataBase Reference: 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol(525-72-4)
• EPA Substance Registry System: 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol(525-72-4)

Safety Data

• Hazardous Substances Data: 525-72-4(Hazardous Substances Data)

Usage

General Description

1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol is a chemical compound with a complex molecular structure. It is a derivative of tetrahydroisoquinoline and contains a methyl group as well as hydroxyl groups. 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol has potential pharmaceutical and biological applications due to its unique structure and properties. Research suggests that it may have antioxidant, anti-inflammatory, and neuroprotective effects, making it a promising candidate for drug development. Further studies are needed to fully understand the potential therapeutic uses of 1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol.

Upstream product

• 63283-42-1 6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 493-48-1 (6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline) 
• 51-61-6 dopamine 
• 75-07-0 acetaldehyde 
• 62-31-7 dopamine hydrochloride 

Downstream Products

• 51-61-6 dopamine 
• 53405-13-3 1,2,3,4-tetrahdyro-1-methylisopquinoline-7,8-diol 
• 4593-97-9 N-Nor-1-methylcorypalline 
• 19641-12-4 6-methoxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-ol 
• 89-31-6 rac-salsoline 
• 114561-80-7 2-benzyl-6,7-bis-benzyloxy-1-methyl-1,2,3,4-tetrahydro-isoquinoline 
• 1581289-16-8 C₁₈H₁₅F₆NO₄S 
• 1581289-14-6 C₁₆H₁₅N₃O₈S 
• 1581289-05-5 C₁₆H₁₅N₃O₈S 
• 65644-76-0 (+/-)-N-Methylsalsoline 
• 490-53-9 (+/-)-carnegine 
• 493-48-1 (6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline) 

Relevant articles and documents

Method for separating and purifying water-soluble catechol type tetrahydroisoquinoline alkaloid by using macroporous resin

The invention provides a method for separating and purifying water-soluble catechol type tetrahydroisoquinoline alkaloid by using a macroporous resin, wherein the water-soluble catechol type tetrahydroisoquinoline alkaloid has a structure represented by a

NEW USE OF ISOQUINOLINE DERIVATIVES FOR WOUND HEALING

The present invention is related to a method for wound healing comprising administering to a subject in need thereof a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound having the general Formula I, preferably salsolinol.

Phosphate mediated biomimetic synthesis of tetrahydroisoquinoline alkaloids

A one-pot synthesis of tetrahydroisoquinoline alkaloids in a phosphate buffer has been achieved, and a reaction mechanism proposed. The utilisation of mild reaction conditions readily afforded a range of isoquinolines, including norcoclaurine.