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1H-Indazole-5-carboxylic acid, 3-iodo-4-methoxy-, ethyl ester is a chemical compound characterized by its molecular formula C12H11IN2O3. It features an indazole ring, an iodine atom, and a methoxy group, which contribute to its versatility as a building block in the synthesis of more complex molecules. 1H-Indazole-5-carboxylic acid, 3-iodo-4-methoxy-, ethyl ester is widely utilized in organic synthesis and drug development, playing a pivotal role in the creation of pharmaceuticals and research chemicals. Its potential biological and pharmacological activities render it a significant compound for further exploration and application within the medical and pharmaceutical sectors.

633327-85-2

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633327-85-2 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indazole-5-carboxylic acid, 3-iodo-4-methoxy-, ethyl ester serves as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with improved therapeutic properties, addressing unmet medical needs.
Used in Organic Synthesis:
As a versatile building block, 1H-Indazole-5-carboxylic acid, 3-iodo-4-methoxy-, ethyl ester is employed in organic synthesis for the creation of more complex molecules. Its presence of an indazole ring, iodine atom, and methoxy group enables the formation of a wide range of chemical compounds with diverse applications.
Used in Drug Development:
1H-Indazole-5-carboxylic acid, 3-iodo-4-methoxy-, ethyl ester is utilized in drug development for the discovery and optimization of new therapeutic agents. Its potential biological and pharmacological activities make it a valuable compound for the design and synthesis of innovative drugs with enhanced efficacy and safety profiles.
Used in Research Chemicals:
1H-Indazole-5-carboxylic acid, 3-iodo-4-methoxy-, ethyl ester is also used in the production of research chemicals, providing scientists and researchers with essential tools for studying biological processes and exploring new avenues in medicinal chemistry. Its unique structural features facilitate the investigation of various chemical and biological phenomena, contributing to the advancement of scientific knowledge in the field.

Check Digit Verification of cas no

The CAS Registry Mumber 633327-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,3,3,2 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 633327-85:
(8*6)+(7*3)+(6*3)+(5*3)+(4*2)+(3*7)+(2*8)+(1*5)=152
152 % 10 = 2
So 633327-85-2 is a valid CAS Registry Number.

633327-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-iodo-4-methoxy-2H-indazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names QC-8304

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:633327-85-2 SDS

633327-85-2Downstream Products

633327-85-2Relevant academic research and scientific papers

PYRAZOLE COMPOUND AND MEDICINAL COMPOSITION CONTAINING THE SAME

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Page/Page column 115, (2008/06/13)

The present invention provides a novel compound having an excellent JNK inhibitory effect. That is, it provides a compound represented by the following formula, a salt thereof or a hydrate of them. Wherein R1 designates -(CO)h-(NRa)j-(CRb=CRc)k-Ar (wherein Ra, Rb and Rc each independently designate a hydrogen atom, a halogen atom, hydroxyl group, an optionally substituted C1-6 alkyl group or the like; Cy designates a 5- or 6-membered heteroaryl; and V each independently designate the formula -L-X-Y (wherein L designates a single bond, an optionally substituted C1-6 alkylene group or the like; X designates a single bond or the formula -A- (wherein A designates NR2, O, CO, S, SO or SO2) and so on; and Y designates a hydrogen atom, a halogen atom, nitro group or the like).

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