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(6-Benzyloxy-1H-indazol-3-yl)-acetic acid is a chemical compound featuring an indazole ring substituted with a benzyloxy group at the 6-position and an acetic acid group at the 3-position. (6-BENZYLOXY-1H-INDAZOL-3-YL)-ACETIC ACID is recognized for its potential in pharmaceutical research and drug development due to the diverse pharmacological properties of the indazole core, such as anti-inflammatory, analgesic, and anticancer activities. The presence of the benzyloxy and acetic acid groups allows for the generation of analogs with enhanced drug-like properties and biological activities, making it a valuable chemical building block for the synthesis of potential therapeutic compounds.

885272-16-2

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885272-16-2 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
(6-Benzyloxy-1H-indazol-3-yl)-acetic acid is used as a chemical building block for the synthesis of potential therapeutic compounds due to its diverse pharmacological properties and the ability to modify the benzyloxy and acetic acid groups to generate analogs with improved drug-like properties and biological activities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-Benzyloxy-1H-indazol-3-yl)-acetic acid is utilized as a starting point for the design and synthesis of new drugs, leveraging its biologically important indazole scaffold and the potential for structural modifications to optimize pharmacokinetic and pharmacodynamic profiles.
Used in Drug Discovery:
(6-Benzyloxy-1H-indazol-3-yl)-acetic acid is employed in drug discovery processes to identify novel compounds with potential therapeutic applications, particularly in areas such as anti-inflammatory, analgesic, and anticancer treatments, by exploring its chemical modifications and interactions with biological targets.
Used in Chemical Synthesis:
In the chemical synthesis industry, (6-Benzyloxy-1H-indazol-3-yl)-acetic acid serves as a key intermediate for the preparation of a variety of complex organic molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals, due to its versatile chemical structure and reactivity.
Used in Biochemical Research:
(6-Benzyloxy-1H-indazol-3-yl)-acetic acid is utilized in biochemical research to study the mechanisms of action of various biologically active compounds, providing insights into the structure-activity relationships and potential therapeutic applications of indazole-based molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 885272-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 885272-16:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*2)+(2*1)+(1*6)=202
202 % 10 = 2
So 885272-16-2 is a valid CAS Registry Number.

885272-16-2SDS

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 2-(6-phenylmethoxy-2H-indazol-3-yl)acetic acid

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:885272-16-2 SDS

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