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3-methoxy-7,9,10,11,11a,12-hexahydrobenzo[f]pyrrolo[1,2-b]isoquinoline is a complex organic compound belonging to the class of benzo[f]pyrrolo[1,2-b]isoquinolines. This molecule is characterized by a hexahydro structure, which means it contains six hydrogen atoms bonded to carbon atoms in a cyclic structure. The presence of a methoxy group (-OCH3) at the 3-position and the fused pyrrolo ring system contribute to its unique chemical properties. 3-methoxy-7,9,10,11,11a,12-hexahydrobenzo[f]pyrrolo[1,2-b]isoquinoline is of interest in the field of organic chemistry, potentially for its pharmacological properties or as a synthetic intermediate in the preparation of more complex molecules. Its specific applications and effects would depend on further research and characterization of its biological activity.

82589-57-9

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82589-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82589-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,8 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82589-57:
(7*8)+(6*2)+(5*5)+(4*8)+(3*9)+(2*5)+(1*7)=169
169 % 10 = 9
So 82589-57-9 is a valid CAS Registry Number.

82589-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxy-7,7a,8,9,10,12-hexahydrobenzo<h>pyrrolo<1,2-b>isoquinoline

1.2 Other means of identification

Product number -
Other names 3-Methoxy-7,9,10,11,11a,12-hexahydrobenzo<f>pyrrolo<1,2-b>isoquinoline

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

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More Details:82589-57-9 SDS

82589-57-9Downstream Products

82589-57-9Relevant academic research and scientific papers

Synthesis of Hexahydropyrroloisoquinolines - Analogs of Phenanthroindolizidine Anticancer Alkaloids

Gaur, S. P.,Jain, Padam C.,Anand, Nitya

, p. 46 - 51 (2007/10/02)

A convenient preparative route has been developed for the synthesis of hexahydropyrroloisoquinolines involving condensation of an araldehyde with ethyl 4-nitrobutanoate followed by LAH reduction and subsequent cyclization with H2SO4 to 2-arylmethylpyrrolidines.The latter on formylation and Bischler-Napieralsky cyclization followed by NaBH4 reduction give the required pyrroloisoquinolines.Using this method, 8-methoxy-1,2,3,5,10,10a-hexahydropyrroloisoquinoline (IXa); 7,8-dimethoxy-1,2,3,5,10,10a-hexahydropyrroloisoquinoline (IXb); 7,9,10,11,11a,12-hexahydrobenzopyrroloisoquinoline (Xa); 3-methoxy-7,9,10,11,11a,12-hexahydrobenzopyrroloisoquinoline (Xb); 7,7a,8,9,10,12-hexahydrobenzopyrroloisoquinoline (XIa); 3-methoxy-7,7a,8,9,10,12-hexahydrobenzopyrroloisoquinoline (XIb) and 2,3-dimethoxy-7,7a,8,9,10,12-hexahydrobenzopyrroloisoquinoline (XIc) have been synthesized.None of these compounds has shown any noteworthy anticancer activity while few have exhibited interesting antihistaminic, β-blocking, hypertensive, antiinflammatory and antireserpine activities.

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