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1,4,6,9-Tetramethyl-3-methoxy-8-hydroxy-11-oxo-11H-dibenzo[b,e][1,4]dioxepin-7-carboxylic acid methyl ester is a complex organic compound with the molecular formula C20H22O7. It is a derivative of dibenzo[b,e][1,4]dioxepin, a type of heterocyclic compound consisting of two benzene rings fused to a dioxepin ring. The structure features four methyl groups, a methoxy group, a hydroxy group, and a carboxylic acid group, which is esterified with a methyl group. 1,4,6,9-Tetramethyl-3-methoxy-8-hydroxy-11-oxo-11H-dibenzo[b,e][1,4]dioxepin-7-carboxylic acid methyl ester is characterized by its unique arrangement of functional groups and may have potential applications in various fields, such as pharmaceuticals or chemical research, due to its specific structural properties.

6161-70-2

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6161-70-2 Usage

Explanation

The compound's name describes its structure, which includes four methyl groups, a methoxy group, a hydroxy group, an oxo group, and a carboxylic acid group.

Explanation

It is a carbon-containing compound, which classifies it as an organic compound.

Explanation

The compound has a fused ring system consisting of two benzene rings and a dioxepane ring.

Explanation

These functional groups contribute to the compound's reactivity and potential applications.

Explanation

It is a synthetic compound, meaning it is not found naturally and is created through chemical synthesis.

Explanation

Due to its complex structure, it may have potential uses in the development of new drugs for various medical conditions.

Explanation

Further research and testing are needed to fully understand the compound's properties and potential uses.

Explanation

The stability of the compound under various conditions is not provided, but it may be affected by factors such as temperature, pH, and exposure to light or air.

Explanation

The toxicity of the compound is not provided, but it should be evaluated before considering its use in pharmaceutical applications.

Type of Compound

Organic compound

Structure

Dibenzo[b,e][1,4]dioxepin

Functional Groups

Methyl ester, methoxy, hydroxy, oxo, and carboxylic acid

Synthetic Compound

Yes

Potential Applications

Pharmaceuticals

Research and Testing

Required

Solubility

Unknown

Stability

Unknown

Toxicity

Unknown

Check Digit Verification of cas no

The CAS Registry Mumber 6161-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6161-70:
(6*6)+(5*1)+(4*6)+(3*1)+(2*7)+(1*0)=82
82 % 10 = 2
So 6161-70-2 is a valid CAS Registry Number.

6161-70-2SDS

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 methyl 8-hydroxy-3-methoxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzo[b,e][1,4]dioxepin-7-carboxylate

1.2 Other means of identification

Product number -
Other names 8-hydroxy-3-methoxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzo[b,e][1,4]dioxepine-7-carboxylic acid methyl ester

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:6161-70-2 SDS

6161-70-2Relevant academic research and scientific papers

Depsidone Synthesis. Part 19. Some β-Orcinol Depsidones

Sala, Tony,Sargent, Melvyn V.

, p. 877 - 882 (2007/10/02)

The synthesis of the lichen depsidones 3,8-dihydroxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzo-dioxepin-7-carboxylic acid (hypoprotocetraric acid) (4), 8-hydroxy-3-methoxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzodioxepin-7-carboxylic acid (

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