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(2S)-Butan-2-yl 2-(3-[4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl]-1-benzofuran-2-yl)acetate is a complex organic compound with a unique molecular structure. It features a butan-2-yl group connected to a benzofuran-2-yl group, which in turn is attached to a 3,5-diiodobenzoyl group and a 2-(diethylamino)ethoxy group. The presence of these functional groups, including the diethylaminoethoxy and diiodobenzoyl moieties, suggests that (2S)-Butan-2-yl 2-(3-[4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl]-1-benzofuran-2-yl)acetate may exhibit a range of pharmacological properties. Its specific applications and effects would depend on the interactions of these functional groups with biological systems.

335148-45-3

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335148-45-3 Usage

Uses

Used in Pharmaceutical Industry:
(2S)-Butan-2-yl 2-(3-[4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl]-1-benzofuran-2-yl)acetate is used as a potential pharmaceutical agent for its diverse pharmacological properties. The presence of the diethylaminoethoxy group may contribute to its interaction with biological targets, such as receptors or enzymes, while the diiodobenzoyl group could enhance its lipophilicity and cellular penetration. The precise therapeutic applications would depend on the specific biological activities of (2S)-Butan-2-yl 2-(3-[4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl]-1-benzofuran-2-yl)acetate.
Used in Research Applications:
In the field of scientific research, (2S)-Butan-2-yl 2-(3-[4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl]-1-benzofuran-2-yl)acetate serves as a valuable tool for studying the structure-activity relationships of complex organic molecules. Its unique functional groups and molecular architecture allow researchers to investigate the effects of specific structural modifications on biological activity, providing insights into the design of novel therapeutic agents.
Used in Drug Delivery Systems:
(2S)-Butan-2-yl 2-(3-[4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl]-1-benzofuran-2-yl)acetate may also be employed in the development of drug delivery systems, leveraging its functional groups to improve the solubility, stability, and bioavailability of therapeutic agents. The diethylaminoethoxy group could potentially enhance water solubility, while the diiodobenzoyl group may contribute to membrane permeability, facilitating the delivery of drugs to their target sites within the body.

Check Digit Verification of cas no

The CAS Registry Mumber 335148-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,1,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 335148-45:
(8*3)+(7*3)+(6*5)+(5*1)+(4*4)+(3*8)+(2*4)+(1*5)=133
133 % 10 = 3
So 335148-45-3 is a valid CAS Registry Number.

335148-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S)-butan-2-yl] 2-[3-[4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl]-1-benzofuran-2-yl]acetate

1.2 Other means of identification

Product number -
Other names Budiodarone (USAN/INN)

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:335148-45-3 SDS

335148-45-3Downstream Products

335148-45-3Relevant academic research and scientific papers

ANTIARRHYTHMIC PRECURSOR COMPOUNDS, METHODS OF SYNTHESIS AND METHODS OF USE

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Page/Page column 35-36, (2008/06/13)

The invention comprises compounds of Formula 1: wherein, R1 is independently H or halogen; R2 is, for example, H or -R10-NR11R12, and wherein R10 is C1-C6 alkyl, and R11 and Rsu

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