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9,10-dimethoxy-8-(trichloromethyl)-5,8-dihydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline is a complex organic compound with a molecular formula of C20H15Cl3NO3. It features a tricyclic structure, with a dihydro-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline core, which is a type of isoquinoline derivative. The molecule is characterized by the presence of two methoxy groups at the 9 and 10 positions, a trichloromethyl group at the 8 position, and a dihydro ring. 9,10-dimethoxy-8-(trichloromethyl)-5,8-dihydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or other chemical products due to its unique structure and properties.

50932-22-4

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50932-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50932-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,3 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50932-22:
(7*5)+(6*0)+(5*9)+(4*3)+(3*2)+(2*2)+(1*2)=104
104 % 10 = 4
So 50932-22-4 is a valid CAS Registry Number.

50932-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-trichloromethyl-7,8-dihydroberberine

1.2 Other means of identification

Product number -
Other names 6H-Benzo[g]-1,3-benzodioxolo[5,6-a]quinolizine,5,8-dihydro-9,10-dimethoxy-8-(trichloromethyl)

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:50932-22-4 SDS

50932-22-4Downstream Products

50932-22-4Relevant academic research and scientific papers

Palmatine and Berberine isolation artifacts

Marek, Radek,Seckarova, Pavlina,Hulova, Dagmar,Marek, Jaromir,Dostal, Jiri,Sklenar, Vladimir

, p. 481 - 486 (2003)

Some 8-substituted derivatives of the protoberberine alkaloids palmatine (1a) and berberine (1b) have been prepared and investigated by 1D and 2D NMR spectroscopy (H-1, C-13, N-15). Complete NMR data for the 8-hydroxy (2), 8-methoxy (3), 8-ethoxy (4), and

The Synthesis and Investigation of New Electroneutral Berberine Derivatives

Burov, Oleg N.,Demekhin, Oleg D.,Kletskii, Mikhail Е.,Kurbatov, Sergey V.,Lisovin, Anton V.,Zagrebaev, Alexander D.

, p. 45 - 57 (2022/02/09)

[Figure not available: see fulltext.] The possibility of obtaining electroneutral 8-substituted berberines was demonstrated experimentally as well as by DFT/B3LYP and ab initio MP2/HF quantum-chemical calculations with the 6-311+G(d,p) basis set. In alkaline media, it is possible to substitute the C-8 position of berberine with such C-nucleophiles as methyl ketones, acetic acid esters, nitriles, geminal di- and trihaloalkanes. This process proceeds stepwise. First, berberine is attacked by a hydroxide anion to form a covalently bonded 8-hydroxyberberine, then 8-hydroxyberberine reacts with a nucleophile in the nonionized (molecular) form.

HYDROPHILIC BERBERINE-TYPE DERIVATIVE AND APPLICATION THEREOF IN PREPARING DRUG

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Paragraph 0059, (2021/02/18)

An 8-dihalomethyl berberine-type quaternary ammonium salt compound represented by general formula (I) or (II) and an application thereof in preparing a drug. The compound shows hydrophilicity and has antimicrobial, anti-inflmmatory, anti-ulcerative colitis, and antitumor activities, while having no or low toxicity.

8-dihalo methylene dihydroberberine compound and anti-infection and anti-inflammatory application thereof

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Paragraph 0050-0051, (2019/11/12)

The invention discloses an 8-dihalo methylene dihydroberberine compound and anti-infection and anti-inflammatory application thereof, and specifically relates to the 8-dihalo methylene dihydroberberine compound shown as the general formula I and physiologically acceptable salt, a synthetic method and application in preparation of a product to prevent, relieve and/or treat microbial infections andinflammation of the 8-dihalo methylene dihydroberberine compound. Compared with a berberine alkaloid quaternary ammonium salt substrate, the 8-dihalo methylene dihydroberberine compound shows significantly enhanced antibacterial activity to gram-positive bacteria and fungus; and pharmacological activity intensity of the 8-dihalo methylene dihydroberberine compound is obviously higher than that ofa control drug, and the 8-dihalo methylene dihydroberberine compound has the advantages of non-toxicity or low toxicity at the same time and can be used for preparing the product to prevent, relieve and/or treat the microbial infections and inflammation.

13,13a-DIHYDROBERBERINE DERIVATIVES, THEIR PHARMACEUTICAL COMPOSITION AND USE

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Page/Page column 18, (2009/07/10)

The present invention provides 13,13a-dihydroberberine derivatives or their physiologically acceptable salts represented by the following formula, pharmaceutical compositions comprising the same, and uses thereof. The 13,13a-dihydroberberine derivatives have an activity of promoting glucose absorption in muscle cells, and the whole animal tests show that the present compounds have effects on improving glucose-tolerance and insulin-resistance, facilitating weight loss, relieving fatty liver and the like. Thus, the present compounds can be used in treating diabetes mellitus, adiposity, fatty liver and complications thereof induced by insulin resistance.

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