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1-[4,7-dimethoxy-6-(2-piperidin-1-ylethoxy)-1-benzofuran-5-yl]-3-ethylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66202-97-9

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66202-97-9 Usage

Chemical structure

A complex chemical compound consisting of a benzofuran ring with two methoxy groups, a piperidine ring, an ethyl group, and a urea moiety.

Molecular weight

Approximately 392.47 g/mol

Appearance

Likely a solid or crystalline substance, though specific appearance may vary depending on the conditions.

Solubility

The solubility of 1-[4,7-dimethoxy-6-(2-piperidin-1-ylethoxy)-1-benzofuran-5-yl]-3-ethylurea is not explicitly mentioned, but it may be soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO) due to its nonpolar nature.

Stability

The stability of 1-[4,7-dimethoxy-6-(2-piperidin-1-ylethoxy)-1-benzofuran-5-yl]-3-ethylurea is not explicitly mentioned, but it may be sensitive to light, heat, or moisture, as many organic compounds with multiple functional groups are.

Pharmacological or biological activity

Likely has specific pharmacological or biological activity due to its complex structure, which may be relevant in medicinal chemistry or pharmaceutical research.

Handling precautions

It is important to handle this chemical with care, as it may have potential hazards or require specific storage conditions. It is also essential to understand its properties before utilization.

Applications

Potential applications in medicinal chemistry or pharmaceutical research, possibly as a drug candidate or a chemical probe for studying biological processes.

Safety

As with any chemical compound, it is crucial to follow proper safety protocols when handling, storing, and using 1-[4,7-dimethoxy-6-(2-piperidin-1-ylethoxy)-1-benzofuran-5-yl]-3-ethylurea, including wearing appropriate personal protective equipment (PPE) and working in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 66202-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66202-97:
(7*6)+(6*6)+(5*2)+(4*0)+(3*2)+(2*9)+(1*7)=119
119 % 10 = 9
So 66202-97-9 is a valid CAS Registry Number.

66202-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4,7-dimethoxy-6-(2-piperidin-1-ylethoxy)-1-benzofuran-5-yl]-3-ethylurea

1.2 Other means of identification

Product number -
Other names -

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:66202-97-9 SDS

66202-97-9Downstream Products

66202-97-9Relevant academic research and scientific papers

Synthesis and Antiarrhythmic Activity of New Benzofuran Derivatives

Bourgery, Guy,Dostert, Philippe,Lacour, Alain,Langlois, Michel,Pourrias, Bernard,Tisne-Versailles, Jacky

, p. 159 - 167 (2007/10/02)

Various 5-aminobenzofuran derivatives were prepared from khellin and screened intravenously in the dog for their potential antiarrhythmic activity against ouabain-induced ventricular arrhythmia and in the Harris test.From systematic structural variations it was found that two methoxy groups in positions 4 and 7 on the benzofuran ring, a tertiary aminoethoxy side chain in position 6, and a N-methylurea group in position 5 led to the most active compounds.These were then tested orally in the Harris test in the dog.The two long-acting derivativesN--N'-methylurea (8j) and N--N'-methylurea (8m) showed advantages when compared to quinidine and diisopyramide and have been selected for further studies.

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