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10089-10-8

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  • TIANFUCHEM-11H-Dibenzo[b,e][1,4]dioxepin-11-one,2,4,7-trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-[(1E)-1-methyl-1-propen-1-yl]-

    Cas No: 10089-10-8

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  • 11H-Dibenzo[b,e][1,4]dioxepin-11-one,2,4,7-trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-[(1E)-1-methyl-1-propen-1-yl]-

    Cas No: 10089-10-8

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  • 11H-Dibenzo[b,e][1,4]dioxepin-11-one,2,4,7-trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-[(1E)-1-methyl-1-propen-1-yl]-

    Cas No: 10089-10-8

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10089-10-8 Usage

Description

2,4,7-Trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one is a complex organic compound characterized by its unique molecular structure. It is a derivative of dibenzo[b,e][1,4]dioxepin-11-one, featuring three chlorine atoms at the 2nd, 4th, and 7th positions, a hydroxyl group at the 3rd position, a methoxy group at the 8th position, and a 1-methyl-1-propenyl group at the 6th position. 2,4,7-Trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one holds potential for various applications due to its distinct chemical properties and structural features.

Uses

Used in Pharmaceutical Industry:
2,4,7-Trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one is used as a pharmaceutical agent for its potential therapeutic effects. The compound's unique structure may allow it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, 2,4,7-Trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one serves as a valuable compound for studying its chemical properties, reactivity, and potential applications in the synthesis of other complex molecules.
Used in Material Science:
The compound may also find use in material science, where its unique structural features could be exploited to develop new materials with specific properties, such as improved stability, reactivity, or selectivity in various applications.
Used in Antimicrobial Applications:
Given its potent and selective antibacterial activity, as seen in related compounds like nidulin, 2,4,7-Trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one may be used as an antimicrobial agent. It could potentially inhibit the growth of harmful bacteria, making it a candidate for use in the development of new antibiotics or antifungal agents.
Used in Anti-inflammatory Applications:
Similar to the related compounds folipasatin and unguinol, 2,4,7-Trichloro-3-hydroxy-8-methoxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one may exhibit anti-inflammatory properties. This could make it a valuable compound for the development of new treatments for inflammation-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 10089-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10089-10:
(7*1)+(6*0)+(5*0)+(4*8)+(3*9)+(2*1)+(1*0)=68
68 % 10 = 8
So 10089-10-8 is a valid CAS Registry Number.

10089-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-but-2-en-2-yl-2,8,10-trichloro-9-hydroxy-3-methoxy-4,7-dimethylbenzo[b][1,4]benzodioxepin-6-one

1.2 Other means of identification

Product number -
Other names 2,4,7-Trichlor-fluoren-9-on-oxim

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:10089-10-8 SDS

10089-10-8Downstream Products

10089-10-8Relevant articles and documents

Semisynthesis and antibacterial activities of nidulin derivatives

Isaka, Masahiko,Yangchum, Arunrat,Supothina, Sumalee,Veeranondha, Sukitaya,Komwijit, Somjit,Phongpaichit, Souwalak

, p. 181 - 184 (2019)

Derivatives of the fungal depsidone, nidulin, have been synthesized in order to evaluate the potential of the chemical skeleton as antibacterial agents. Alkylation, acylation, and arylation reactions of nornidulin underwent in a regioselective manner to p

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