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3-(4-methoxyphenyl)-1H-indol-5-amine, also known as 4-methoxy-1H-indol-5-ylamine, is a chemical compound with the molecular formula C15H14N2O. It is an amine derivative of indole, a heterocyclic aromatic organic compound. 3-(4-methoxyphenyl)-1H-indol-5-amine is characterized by its potential to be a building block in the synthesis of various biologically active molecules, including pharmaceuticals and agrochemicals.

770701-75-2

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770701-75-2 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-methoxyphenyl)-1H-indol-5-amine is used as a key intermediate in the synthesis of drugs targeting serotonin receptors and enzymes. Its structural features allow for the development of compounds that can modulate these biological targets, which are implicated in a range of disorders, including depression, anxiety, and other mood-related conditions.
Used in Drug Discovery and Development:
3-(4-methoxyphenyl)-1H-indol-5-amine is utilized as a starting material for the creation of new drug candidates. Its presence in the molecular structure can influence the pharmacological properties of the resulting compounds, making it a valuable component in the design and synthesis of novel therapeutic agents.
Used in Anticancer Research:
3-(4-methoxyphenyl)-1H-indol-5-amine is studied for its potential anticancer properties. Its ability to interact with cellular targets and disrupt cancer cell processes makes it a candidate for further research into the development of cancer treatments.
Used in Antimicrobial Applications:
3-(4-methoxyphenyl)-1H-indol-5-amine is also being investigated for its antimicrobial properties. Given the increasing prevalence of antibiotic-resistant bacteria, 3-(4-methoxyphenyl)-1H-indol-5-amine may offer a new avenue for the development of antimicrobial agents.
Used in Organic Synthesis:
3-(4-methoxyphenyl)-1H-indol-5-amine is used as a building block in organic synthesis, allowing for the creation of a variety of complex organic molecules. Its versatility in chemical reactions makes it a valuable component in the synthesis of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 770701-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,0,7,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 770701-75:
(8*7)+(7*7)+(6*0)+(5*7)+(4*0)+(3*1)+(2*7)+(1*5)=162
162 % 10 = 2
So 770701-75-2 is a valid CAS Registry Number.

770701-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenyl)-1H-indazol-5-amine

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 -
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More Details:770701-75-2 SDS

770701-75-2Downstream Products

770701-75-2Relevant academic research and scientific papers

Efficient synthesis of 3-aryl-1H-indazol-5-amine by Pd-catalyzed Suzuki-Miyaura cross-coupling reaction under microwave-assisted conditions

Wang, Shengqiang,Guo, Ruiyun,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng

, p. 3750 - 3753 (2015/06/08)

Various 3-aryl-1H-indazol-5-amine derivatives were synthesized by Pd-catalyzed Suzuki-Miyaura cross-coupling reaction of (NH) free 3-bromo-indazol-5-amine with arylboronic acids under microwave-assisted conditions. The coupling reaction can be carried out under the conditions with dioxane/H2O as solvent, Pd(OAc)2 and RuPhos as catalyst system, and K3PO4 as a base in good to excellent yields.

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