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Ethyl 1,2,9,10-tetramethoxy-4,5-dihydro-6H-dibenzo[de,g]quinoline-6-carboxylate is a complex organic compound with the molecular formula C21H23NO6. It belongs to the class of dibenzo[de,g]quinolines, which are a type of tricyclic aromatic compounds. This specific compound features a quinoline core with a dihydro structure, indicating the presence of a saturated carbon-carbon bond within the ring system. The molecule is further characterized by four methoxy groups (-OCH3) attached to the 1, 2, 9, and 10 positions, and a carboxylate group (-COO-) at the 6 position, which is esterified with an ethyl group (-CH2CH3). This chemical structure endows the compound with unique electronic and steric properties, which can be relevant in various chemical and pharmaceutical applications, such as the development of potential therapeutic agents or as intermediates in the synthesis of more complex molecules.

7630-72-0

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7630-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7630-72-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,3 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7630-72:
(6*7)+(5*6)+(4*3)+(3*0)+(2*7)+(1*2)=100
100 % 10 = 0
So 7630-72-0 is a valid CAS Registry Number.

7630-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-N-ethoxycarbonyldehydronorglaucine

1.2 Other means of identification

Product number -
Other names N-Ethoxycarbonyl-6a,7-dehydro-N-norglaucin

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:7630-72-0 SDS

7630-72-0Downstream Products

7630-72-0Relevant academic research and scientific papers

New N-substituted (±)-dehydronorglaucine analogs

Benedetti-Doctorovich,Huang,Lambropoulos,Burgess,Zalkow

, p. 3701 - 3709 (1995)

The aporphine alkaloid N-carbethoxydehydronorglaucine (1) was found to have promising in vitro antitumor activity, but poor water solubility. We report the synthesis of 1, the efficient hydrolysis of its urethane group and the further transformation into several new dehydronorglaucine analogs.

PHOTOCHEMICAL SYNTHESIS OF APORPHINES: (+/-)-GLAUCINE, (+/-)-NORGLAUCINE AND (+/-)-DEHYDRONORGLAUCINE

Gupta, Sandeep,Bhakuni, Dewan S.

, p. 393 - 402 (2007/10/02)

Photochemical cyclization of 3 afforded 5, 4 and 8. 5 on LAH reduction furnished (+/-)-glaucine (6) and on treatment with ethanolic HCl afforded (+/-)-norglaucine (7). 10 obtained by the photocyclization of 9 was converted into 7 and 11 via 12.

OXIDATION OF APORPHINES BY TRIPLET BENZOPHENONE

Castedo, Luis,Iglesias, Teresa,Puga, Alberto,Saa, Jose M.,Suau, Rafael

, p. 915 - 918 (2007/10/02)

A mild and efficient method to dehydrogenate nonphenolic and phenolic aporphine and noraporphine alkaloids is described.It is based on the photoreduction of benzophenone by amines.

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