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4-AMINOMETHYL-2-PHENYL-OXAZOLEHYDROCHLORIDE is a chemical compound characterized by an oxazole ring with an aminomethyl and a phenyl group attached to it. It is recognized for its stability and non-toxicity, making it a valuable component in pharmaceutical research and drug development.

33105-95-2

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33105-95-2 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
4-AMINOMETHYL-2-PHENYL-OXAZOLEHYDROCHLORIDE is used as a building block for the synthesis of various bioactive compounds, including potential drugs and pharmaceutical intermediates. Its unique structure allows for the creation of new chemical entities with therapeutic potential.
Used in Anti-inflammatory and Analgesic Applications:
In preclinical studies, 4-AMINOMETHYL-2-PHENYL-OXAZOLEHYDROCHLORIDE has demonstrated potential as an anti-inflammatory and analgesic agent, making it a candidate for further research and development in the treatment of pain and inflammation.
Used in Organic Synthesis:
4-AMINOMETHYL-2-PHENYL-OXAZOLEHYDROCHLORIDE is utilized as a reagent in organic synthesis to form new chemical structures with potential biological activity. Its versatility in forming different chemical entities contributes to the discovery of novel compounds with therapeutic applications.
Used in Chemical Research:
Due to its stability and non-toxic nature, 4-AMINOMETHYL-2-PHENYL-OXAZOLEHYDROCHLORIDE is considered a valuable tool in chemical research, facilitating the exploration of new chemical reactions and the development of innovative synthetic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 33105-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33105-95:
(7*3)+(6*3)+(5*1)+(4*0)+(3*5)+(2*9)+(1*5)=82
82 % 10 = 2
So 33105-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O.ClH/c11-6-9-7-13-10(12-9)8-4-2-1-3-5-8;/h1-5,7H,6,11H2;1H

33105-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-AMINOMETHYL-2-PHENYL-OXAZOLEHYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names C-(2-phenyl-oxazol-4-yl)-methylamine,monohydrochloride

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:33105-95-2 SDS

33105-95-2Downstream Products

33105-95-2Relevant academic research and scientific papers

Design, Synthesis and Biological Evaluation of N-((2-phenyloxazol-4-yl)methyl) Pyrimidine Carboxamide Derivatives as Potential Fungicidal Agents

Huang, Danling,Zheng, Shumin,Cheng, Yong-Xian

, p. 185 - 191 (2021/02/12)

Twelve N-((2-phenyloxazol-4-yl)methyl) pyrimidine carboxamide derivatives were designed, synthesized, and characterized by 1H NMR, 13C NMR, and HRMS. The fungicidal activities of these new compounds against Sclerotinia sclerotiorum, Botrytis cinereal, and Colletotrichum fragariae were evaluated. The results indicated that compounds 5b, 5f, and 5g displayed potential fungicidal activities against tested fungi, especially 5f exhibited IC50 value of 28.9 mg/L against S. sclerotiorum. Moreover, the compounds 5f and 5g showed IC50 values of 54.8 mg/L and 62.2 mg/L against C. fragariae respectively, which shows that they were more active than the commercial fungicide hymexazol. The superficial structure-activity relationships were discussed, which may be of benefit for the development of fungicides and discovery of novel fungicides.

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