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(8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinoline-1,2-diyl)dimethanediyl bis(cyclohexylcarbamate) is a complex chemical compound characterized by the presence of various functional groups, including a methoxy group, a methyl group, a dihydropyrroloisoquinoline group, dimethanediyl, and bis(cyclohexylcarbamate) moieties. The intricate molecular structure and the combination of these functional groups suggest that the compound may exhibit a range of pharmacological or biological properties, making it a candidate for potential applications in medicinal chemistry and drug development.

91523-56-7

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91523-56-7 Usage

Uses

Used in Pharmaceutical Industry:
(8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinoline-1,2-diyl)dimethanediyl bis(cyclohexylcarbamate) is used as a potential therapeutic agent for various medical conditions due to its complex molecular structure and the presence of multiple functional groups that may interact with biological targets.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinoline-1,2-diyl)dimethanediyl bis(cyclohexylcarbamate) is used as a compound of interest for studying its pharmacological properties and potential interactions with biological systems. (8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinoline-1,2-diyl)dimethanediyl bis(cyclohexylcarbamate)'s structure may provide insights into the design of new drugs with specific therapeutic effects.
Used in Drug Development:
(8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinoline-1,2-diyl)dimethanediyl bis(cyclohexylcarbamate) is utilized in drug development as a starting point for the synthesis of new drug candidates. (8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinoline-1,2-diyl)dimethanediyl bis(cyclohexylcarbamate)'s unique structure and functional groups may be modified or used as a template to create novel therapeutic agents with improved efficacy and selectivity.
Used in Chemical Synthesis:
In the chemical synthesis industry, (8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinoline-1,2-diyl)dimethanediyl bis(cyclohexylcarbamate) may be used as a building block or intermediate in the synthesis of more complex molecules with specific applications in various fields, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 91523-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,2 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91523-56:
(7*9)+(6*1)+(5*5)+(4*2)+(3*3)+(2*5)+(1*6)=127
127 % 10 = 7
So 91523-56-7 is a valid CAS Registry Number.

91523-56-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(cyclohexylcarbamoyloxymethyl)-8-methoxy-3-methyl-5,6-dihydropyrrolo[2,1-a]isoquinolin-2-yl]methyl N-cyclohexylcarbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,(5,6-dihydro-8-methoxy-3-methylpyrrolo[2,1-a]isoquinolne-1,2-diyl)bis(methylene) ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91523-56-7 SDS

91523-56-7Downstream Products

91523-56-7Relevant academic research and scientific papers

Synthesis and Murine Antineoplastic Activity of Bis Derivatives of Pyrroloisoquinoline

Anderson, Wayne K.,McPherson, Howard L.,New, James S.,Rick, Arvela C.

, p. 1321 - 1325 (2007/10/02)

The synthesis of 4,5-dihydropyrroloisoquinolines is reported.A key intermediate in the synthesis of 8-methoxy-4,5-dihydropyrroloisoquinolines, 6-hydroxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (6), was prepared by using a regiospeci

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