38449-59-1

Basic information

• Product Name: M-TyraMine HydrobroMide
• Synonyms: M-TyraMine HydrobroMide
• CAS NO: 38449-59-1
• Molecular Formula: BrH*C₈H₁₁NO
• Molecular Weight: 218.09098
• Mol File: 38449-59-1.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: M-TyraMine HydrobroMide(CAS DataBase Reference)
• NIST Chemistry Reference: M-TyraMine HydrobroMide(38449-59-1)
• EPA Substance Registry System: M-TyraMine HydrobroMide(38449-59-1)

Safety Data

• Hazardous Substances Data: 38449-59-1(Hazardous Substances Data)

Usage

Uses

Brain microsomes were able to metabolize tyramine to dopamine.

Upstream product

• 2039-67-0 2-(3-methoxyphenyl)-1-ethanamine 
• 19924-43-7 3-methoxyphenylacetonitrile 
• 874-98-6 1-bromomethyl-3-methoxybenzene 
• 100-84-5 1-methoxy-3-methyl-benzene 

Downstream Products

• 91523-50-1 rac-6-hydroxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid 
• 780004-18-4 ethyl (1SR)-6-hydroxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylate 
• 305822-95-1 4H-Benzo[a]quinolizin-4-one, 1,2,3,6,7,11b-hexahydro-9-hydroxy-11b-(phenylmethyl)- 
• 350014-18-5 1,2,3,4-Tetrahydro-6-hydroxy-1-isoquinolinecarboxylic acid methyl ester 
• 1361226-18-7 N⁽¹⁾-(4-butylphenyl)-N⁽²⁾-(3-hydroxyphenethyl)phthalamide 
• 132513-29-2 tert-butyl {2-[3-(benzyloxy)phenyl]ethyl}carbamate 
• 29973-97-5 2-(3-benzyloxyphenyl)ethyl amine hydrochloride 
• 1443827-86-8 C₂₄H₂₃NO₃ 
• 1443827-78-8 N-(3-(benzyloxy)phenylethyl)-2-chloroacetamide 
• 1443827-79-9 N-(3-(benzyloxy)phenethyl)-2-(4-methoxyphenoxy)acetamide 
• 1443828-16-7 (6-(benzyloxy)-1-((4-methoxyphenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)(phenyl)methanone 
• 1443828-17-8 (6-(benzyloxy)-1-((4-methoxyphenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)(3-chlorophenyl)methanone 
• 1443828-18-9 (6-(benzyloxy)-1-((4-methoxyphenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)(3-bromophenyl)methanone 
• 1443828-02-1 6-(benzyloxy)-1-((4-methoxyphenoxy)methyl)-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Tetrahydroisoquinoline compound as estrogen receptor and histone deacetylase double-target compound, and synthesis method and application thereof

The invention discloses a tetrahydroisoquinoline compound as an estrogen receptor and histone deacetylase double-target compound as well as a synthesis method and application of the tetrahydroisoquinoline compound. The compound can target an estrogen rece

One-pot chemoenzymatic synthesis of trolline and tetrahydroisoquinoline analogues

Chemoenzymatic reaction cascades can provide access to chiral compounds from low-cost starting materials in one pot. Here we describe one-pot asymmetric routes to tetrahydroisoquinoline alkaloids (THIAs) using the Pictet-Spenglerase norcoclaurine synthase (NCS) followed by a cyclisation, to give alkaloids with two new heterocyclic rings. These reactions operated with a high atom economy to generate THIAs in high yields.

Synthesis and structure activity relationship of tetrahydroisoquinoline- based potentiators of GluN2C and GluN2D containing N-Methyl-D-aspartate receptors

We describe here the synthesis and evaluation of a series of tetrahydroisoquinolines that show subunit-selective potentiation of NMDA receptors containing the GluN2C or GluN2D subunits. Bischler-Napieralski conditions were employed in the key step for the