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3-methoxy-6-methyl-8,9,10,11-tetrahydro-1H-indolo[3,2-c]quinoline-1,4(7H)-dione is a complex organic compound belonging to the class of indoloquinoline derivatives. It features a tricyclic structure with a quinoline ring fused to an indolo ring, and it is characterized by the presence of a 3-methoxy group and a 6-methyl group. The compound is a tetrahydro derivative, indicating that it has four hydrogen atoms added across the molecule, and it possesses a 1,4-dione functional group, which consists of two carbonyl groups (C=O) at the 1st and 4th positions. This chemical is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or materials science due to its unique structure and properties.

113698-18-3

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113698-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113698-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,9 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113698-18:
(8*1)+(7*1)+(6*3)+(5*6)+(4*9)+(3*8)+(2*1)+(1*8)=133
133 % 10 = 3
So 113698-18-3 is a valid CAS Registry Number.

113698-18-3SDS

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 3-methoxy-6-methyl-8,9,10,11-tetrahydro-7H-indolo[3,2-c]quinoline-1,4-dione

1.2 Other means of identification

Product number -
Other names 1H-Indolo(3,2-c)quinoline-1,4(7H)-dione,8,9,10,11-tetrahydro-3-methoxy-6-methyl

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:113698-18-3 SDS

113698-18-3Downstream Products

113698-18-3Relevant academic research and scientific papers

Heterocyclic quinones VIII. Synthesis and anti-neoplastic evaluation of 7-substituted-1H-pyrroloquinoline-6,9-diones and 3-substituted-11H-indoloquinoline-1,4-diones

Helissey, Philippe,Parrot-Lopez, Helene,Renault, Jean,Cros, Suzanne,Paoletti, Claude

, p. 277 - 282 (2007/10/02)

7-Methoxy-2,3,4-trimethyl-1H-pyrroloquinoline-6,9-dione 13 and 3-methoxy-6-methyl-11H-indoloquinoline-1,4-diones 15 and 19 were obtained by oxidation of quinolinamines 9, 11 and 12 with Fremy's salt.The synthesis method of amines 9 and 11 consists of creating the pyrrole or indole nucleus according to Fischer's indolic reaction applied to hydrazones 8 and 10.Aromatization of 11 yielded quinolinamine 12.The nucleophilic substitution of methoxy by aziridine leads to quinones 14, 16 and 20.These quinones are highly cytotoxic for L1210 cells, but no activity could be established for the P388 lymphocytic leukemia in vivo.Keywords: anti-tumor agents / cytotoxicity / Fischer indolic reaction / Fremy's salt / heterocyclic quinones / 11H-indoloquinoline-1,4-diones / 1H-pyrroloquinoline-6,9-diones / P388 lymphocytic leukemia

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