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1,2-dimethyl-3,4-dihydro-1H-isoquinoline-6,7-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53622-84-7

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53622-84-7 Usage

Molecular Structure

A complex structure with a dihydroisoquinoline core, featuring two methyl groups at positions 1 and 2, and two hydroxyl groups at positions 6 and 7.

Class

Isoquinoline class of compounds

Substitution Pattern

Dihydroxy

Pharmacological Properties

TIQ has been studied for its potential to modulate the central nervous system and dopamine receptors.

Potential Applications

TIQ has been investigated for its potential use in the treatment of drug addiction and withdrawal symptoms.

Research Interest

TIQ's unique structure and potential medicinal properties make it an interesting compound for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 53622-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,2 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53622-84:
(7*5)+(6*3)+(5*6)+(4*2)+(3*2)+(2*8)+(1*4)=117
117 % 10 = 7
So 53622-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-7-9-6-11(14)10(13)5-8(9)3-4-12(7)2/h5-7,13-14H,3-4H2,1-2H3/t7-/m1/s1

53622-84-7Downstream Products

53622-84-7Relevant academic research and scientific papers

Monitoring on-chip pictet-spengler reactions by integrated analytical separation and label-free time-resolved fluorescence

Ohla, Stefan,Beyreiss, Reinhild,Fritzsche, Stefanie,Glaser, Petra,Nagl, Stefan,Stockhausen, Kai,Schneider, Christoph,Belder, Detlev

supporting information; experimental part, p. 1240 - 1246 (2012/03/26)

High-throughput screening for optimal reaction conditions and the search for efficient catalysts is of eminent importance in the development of chemical processes and for expanding the spectrum of synthetic methodologies in chemistry. In this context we report a novel approach for a microfluidic chemical laboratory integrating organic synthesis, separation and time-resolved fluorescence detection on a single microchip. The feasibility of our integrated laboratory is demonstrated by monitoring the formation of tetrahydroisoquinoline derivatives by Pictet-Spengler condensation. After on-chip reaction the products and residual starting material were separated enantioselectively on the same chip. On-chip deep UV laser-induced fluorescence detection with time-correlated single photon counting was applied for compound assignment. The system was utilized to screen reaction conditions and various substrates for Pictet-Spengler reactions on-chip. Finally, the microlab was successfully applied to investigate enantioselective reactions using BINOL-based phosphoric acids as organocatalysts. Chip trick: An integrated chip-based approach for rapid monitoring of organic synthesis at the microscale level is presented. This is achieved by the integration of microfluidic channels for reaction and electrophoresis on a single device together with time-correlated single-photon counting for compound identification (see figure). Copyright

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