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2-Oxazolamine, 4-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68101-28-0

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68101-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68101-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,0 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68101-28:
(7*6)+(6*8)+(5*1)+(4*0)+(3*1)+(2*2)+(1*8)=110
110 % 10 = 0
So 68101-28-0 is a valid CAS Registry Number.

68101-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methoxy-phenyl)-oxazol-2-ylamine

1.2 Other means of identification

Product number -
Other names 2-Amino-5-(4-methoxy-phenyl)-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:68101-28-0 SDS

68101-28-0Relevant academic research and scientific papers

Synthesis, Characterization, and Antioxidant Activity of a New Class of Amido linked Azolyl Thiophenes

Thatha, Sreenivasulu,Ummadi, Nagarjuna,Venkatapuram, Padmavathi,Adivireddy, Padmaja

, p. 1410 - 1418 (2018)

A new class of amido linked azolyl thiophenes was prepared from the synthetic intermediates azolyl amines and 5-chlorothiophene-2-carbonyl chloride adopting conventional and ultrasonication methodologies. It was observed that the reaction took place in shorter reaction times with higher yields under ultrasonication. The structures of the synthesized compounds were characterized by spectral parameters and also tested for antioxidant activity. Among all the tested compounds, methoxy substituted oxazolyl thiophene carboxamide (8c) displayed promising antioxidant activity. Besides, the electron donating groups on the phenyl ring enhanced the antioxidant activity when compared with the electron withdrawing groups.

2-Aminooxazole as a Novel Privileged Scaffold in Antitubercular Medicinal Chemistry

Annunziato, Giannamaria,Azzali, Elisa,Costantino, Gabriele,Girardini, Miriam,Mori, Giorgia,Pasca, Maria Rosalia,Pavone, Marialaura,Pieroni, Marco,Vacondio, Federica

supporting information, p. 1435 - 1441 (2020/08/19)

To obtain effective eradication of numerous infectious diseases such as tuberculosis, it is important to supply the medicinal chemistry arsenal with novel chemical agents. Isosterism and bioisosterism are widely known concepts in the field of early drug d

Comparative material study and synthesis of 4-(4-nitrophenyl)oxazol-2-amine via sonochemical and thermal method

Singh, Balvant S.,Lobo, Hyacintha R.,Pinjari, Dipak V.,Jarag, Krishna J.,Pandit, Aniruddha B.,Shankarling, Ganapati S.

, p. 633 - 639 (2013/02/22)

The present paper deals with the synthesis of aminooxazole derivatives via thermal and ultrasonic methods using deep eutectic solvent as medium. It was observed that ultrasound-assisted method gave 90% yield in just 8 min as against 3.5 h required to get

COMPOUNDS FOR THE INHIBITION OF CELLULAR PROLIFERATION

-

Page/Page column 85, (2012/02/01)

Compositions and methods for inhibiting translation are provided. Compositions, methods and kits for treating (1) cellular proliferative disorders, (2) non-proliferative, degenerative disorders, (3) viral infections, (4) disorders associated with viral infections, and/or (5) non-proliferative metabolic disorders such as type II diabetes where inhibition of translation initiation is beneficial using the compounds disclosed herein.

A novel and efficient one pot synthesis of 2,4-disubstituted thiazoles and oxazoles using phenyltrimethylammoniumtribromide in ionic liquid

Muthyala, Manoj Kumar,Kumar, Anil

, p. 959 - 964 (2012/10/29)

A novel and efficient one-pot procedure has been described for synthesis of 2,4-disubstituted thiazoles and oxazoles from substituted ketones using phenyltrimethylammoniumtribromide as in situ brominating agent followed by reaction with thioamide/thiourea and amides/ureas, respectively in [bmim][BF4] ionicliquid. The advantages of the procedure include avoiding the handling of lacrymetric compounds, hazardous and toxic organic solvents along with good to excellent yield of the products.

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