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2-Methylnaphth[2,3-d]oxazole is a chemical compound that belongs to the class of organic compounds known as oxazoles. Oxazoles are compounds that contain an oxazole ring, which is a five-membered aromatic ring featuring one oxygen atom, one nitrogen atom, and three carbon atoms. This specific compound has a methyl group attached to the naphthalene core, which contributes to its unique chemical properties. It has been reported to have potential carcinogenic properties, but additional research is needed to confirm this. The properties and exact physiological effects of 2-Methylnaphth[2,3-d]oxazole on human or environmental health are not well-understood and warrant further investigation.

20686-66-2

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20686-66-2 Usage

Uses

Used in Organic Chemistry Research:
2-Methylnaphth[2,3-d]oxazole is used as a research compound for studying the properties and potential applications of oxazole-containing compounds. Its unique structure and potential carcinogenic properties make it an interesting subject for further investigation in the field of organic chemistry.
Used in Chemical Synthesis:
2-Methylnaphth[2,3-d]oxazole can be synthesized through a complex chemical process, which may involve the use of various reagents and reaction conditions. This synthesis process is of interest to researchers in the field of organic chemistry, as it may provide insights into the development of new synthetic methods and the creation of novel compounds with potential applications in various industries.
Used in Toxicological Studies:
Due to the reported potential carcinogenic properties of 2-Methylnaphth[2,3-d]oxazole, it may be used as a subject in toxicological studies to better understand its effects on human health and the environment. These studies can help determine the safety and potential risks associated with exposure to 2-METHYLNAPHTH[2,3-D]OXAZOLE, as well as inform regulatory decisions and guidelines for its use in various applications.
Used in Pharmaceutical Research:
Although the exact physiological effects of 2-Methylnaphth[2,3-d]oxazole on human health are not well-understood, its unique structure and potential biological activity may make it a candidate for pharmaceutical research. Researchers may investigate its potential as a therapeutic agent or as a starting point for the development of new drugs with specific pharmacological properties. Further research is needed to explore these possibilities and to better understand the potential benefits and risks associated with the use of 2-Methylnaphth[2,3-d]oxazole in pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 20686-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,8 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20686-66:
(7*2)+(6*0)+(5*6)+(4*8)+(3*6)+(2*6)+(1*6)=112
112 % 10 = 2
So 20686-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO/c1-8-13-11-6-9-4-2-3-5-10(9)7-12(11)14-8/h2-7H,1H3

20686-66-2 Well-known Company Product Price

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  • Alfa Aesar

  • (B21806)  2-Methylnaphtho[2,3-d]oxazole, 98%   

  • 20686-66-2

  • 5g

  • 639.0CNY

  • Detail
  • Alfa Aesar

  • (B21806)  2-Methylnaphtho[2,3-d]oxazole, 98%   

  • 20686-66-2

  • 25g

  • 2417.0CNY

  • Detail

20686-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylbenzo[f][1,3]benzoxazole

1.2 Other means of identification

Product number -
Other names 2-Methylnaphtho[2,3-d]oxazole

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:20686-66-2 SDS

20686-66-2Downstream Products

20686-66-2Relevant academic research and scientific papers

Ethoxymethylenemalonates and Malononitriles (EMM reagents) as formic acid equivalents: Synthesis of fused-imidazoles under neutral or mildly acidic con

Segelstein, Barb E.,Chenard, Bert L.,Macor, John E.,Post, Ronald J.

, p. 1897 - 1900 (2007/10/02)

The use of ethoxymethylenemalonates and malononitriles (EMM reagents) for the efficient synthesis of fused imidazoles and related compounds is describe.

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