Welcome to LookChem.com Sign In|Join Free
  • or
2-Oxazolamine, 4-(1,1-dimethylethyl)-, also known as tert-butyl 4-oxazolidinecarboxylate, is a chemical compound with the molecular formula C8H14N2O. It is a derivative of oxazolamine and is recognized for its versatile reactivity and potential for biological activity. 2-OxazolaMine, 4-(1,1-diMethylethyl)is commonly utilized as a building block in organic synthesis and pharmaceutical research, and has been studied for its potential antimicrobial and anticancer properties, positioning it as a significant focus in the field of medicinal chemistry.

97567-79-8

Post Buying Request

97567-79-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

97567-79-8 Usage

Uses

Used in Pharmaceutical Research and Organic Synthesis:
2-Oxazolamine, 4-(1,1-dimethylethyl)is used as a building block in pharmaceutical research and organic synthesis for its versatile reactivity and potential for biological activity. Its unique structure allows it to be a key component in the development of new pharmaceuticals and agrochemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Oxazolamine, 4-(1,1-dimethylethyl)is used for its potential antimicrobial and anticancer properties. Researchers are exploring its applications in the development of new treatments and therapies, particularly for cancer and infectious diseases.
Used in the Production of Pharmaceuticals and Agrochemicals:
2-Oxazolamine, 4-(1,1-dimethylethyl)is also utilized in the production of various pharmaceuticals and agrochemicals. Its presence in these products is attributed to its ability to contribute to the effectiveness and functionality of the final compounds.
The specific applications and industries where 2-Oxazolamine, 4-(1,1-dimethylethyl)is used may vary, but its role as a versatile building block in the creation of new compounds for health and agriculture is well-established. Further research and development will likely uncover additional uses and enhance its importance in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 97567-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 97567-79:
(7*9)+(6*7)+(5*5)+(4*6)+(3*7)+(2*7)+(1*9)=198
198 % 10 = 8
So 97567-79-8 is a valid CAS Registry Number.

97567-79-8SDS

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-tert-butyl-1,3-oxazol-2-amine

1.2 Other means of identification

Product number -
Other names QC-4986

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:97567-79-8 SDS

97567-79-8Relevant academic research and scientific papers

INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS

-

Page/Page column 16, (2012/03/10)

This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases, other than cancer and proteolytic enzyme mediated diseases, other than cancer, and pharmaceutical compositions for use in such therapy.

INHIBITION OF RAF KINASE USING SUBSTITUTED HETEROCYCLIC UREAS

-

Page/Page column 16, (2010/11/28)

Methods of treating tumors mediated by raf kinase, with substituted urea compounds, and such compounds per se.

Formation of Thioamide Derivatives from Reactions of Isothiocyanates with Oxazol-2-amines

Crank, George,Khan, Humaid R.

, p. 447 - 458 (2007/10/02)

4-Substituted oxazol-2-amines react with isothiocyanates to give products having a thioamide function at C5.The reaction is considered to be an electrophilic process in competition with the usual reaction of the amino group with the isothiocyanate.The nature of the isothiocyanate and the type of substituent at C4 affect the amount of the thioamide product formed.Some chemical properties of the thioamides are also investigated.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 97567-79-8