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6-Methoxyl-2-aminobenzoxazol is a chemical compound belonging to the benzoxazole family, characterized by the presence of a methoxy group and an amino group attached to the benzoxazole ring. It has been studied for its potential biological and pharmacological activities, including its potential as an anti-cancer agent and its ability to inhibit enzyme activity. Additionally, it has been investigated for its use as a fluorescent dye in biological imaging. The presence of both a methoxy and amino group in its structure gives 6-Methoxyl-2-aMinobenzoxazol unique properties that make it potentially useful in various applications in the fields of medicine and biomedical research.

13895-08-4

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13895-08-4 Usage

Uses

Used in Pharmaceutical Industry:
6-Methoxyl-2-aminobenzoxazol is used as a potential anti-cancer agent for its ability to inhibit tumor growth and progression. It modulates several oncological signaling pathways, making it a promising candidate for cancer treatment.
Used in Biomedical Research:
6-Methoxyl-2-aminobenzoxazol is used as a fluorescent dye in biological imaging due to its unique properties. This allows researchers to visualize cellular structures and processes, aiding in the study of various biological phenomena.
Used in Enzyme Inhibition:
6-Methoxyl-2-aminobenzoxazol is used as an enzyme inhibitor, blocking the activity of specific enzymes involved in various biological processes. This can be useful in the development of drugs targeting specific enzyme-related diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 13895-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13895-08:
(7*1)+(6*3)+(5*8)+(4*9)+(3*5)+(2*0)+(1*8)=124
124 % 10 = 4
So 13895-08-4 is a valid CAS Registry Number.

13895-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-1,3-benzoxazol-2-amine

1.2 Other means of identification

Product number -
Other names 6-methoxy-benzooxazol-2-ylamine

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:13895-08-4 SDS

13895-08-4Relevant academic research and scientific papers

Design and synthesis of novel benzoxazole analogs as Aurora B kinase inhibitors

An, Ying,Lee, Eun,Yu, Yeongji,Yun, Jieun,Lee, Myeong Youl,Kang, Jong Soon,Kim, Woo-Young,Jeon, Raok

supporting information, p. 3067 - 3072 (2016/06/13)

A novel series of benzoxazole analogs was designed and synthesized, and their inhibitory activities against Aurora kinases were evaluated. Some of the tested compounds exhibited a promising activity with respect to the inhibition of Aurora B kinase. A structure-activity relationship study indicated that linker length, regiochemistry, and halogen substitution play important roles in kinase inhibitory potency. The binding modes between representative compounds and Aurora kinases were interpreted through a molecular docking study to explain the inhibitory activity and selectivity for Aurora A and B kinases. Compounds 13l and 13q also show an antiproliferative effect on the human tumor cell lines in a dose-dependent manner. The most potent 13q demonstrated good efficacy in the prostate cancer PC-3 tumor xenograft model.

Α 7 as intranuclear hydroxynicotinic acetylcholine receptor quinuclidines compd.

-

Paragraph 0667; 0668, (2018/10/03)

PROBLEM TO BE SOLVED: To provide ligands for the nicotinic α-7 receptor used for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.SOLUTION: The disclosure provides compounds of the specified formula I, including their salts, and compositions and methods using the compounds.

A facile synthesis of 2-aminobenzoxazoles and 2-aminobenzimidazoles using N -cyano- N -phenyl- P -toluenesulfonamide (NCTS) as an efficient electrophilic cyanating agent

Kasthuri, Mahesh,Babu, H. Sharath,Kumar, K. Shiva,Sudhakar, Ch.,Kumar, P. V. Nagendra

, p. 897 - 900 (2015/04/27)

A facile synthesis of 2-aminobenzoxazole and 2-aminobenzimidazole derivatives employing a nonhazardous electrophilic cyanating agent: N-cyano-N-phenyl-p-toluenesulfonamide (NCTS) with various substituted 2-aminophenols and benzene-1,2-diamine derivatives in the presence of lithium hexamethyldisilazide (LiHMDS) is described. This novel protocol boasts operational simplicity, shorter reaction time, and simple workup.

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