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5-Bromo-2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester is a chemical compound characterized by the molecular formula C13H16BrN3O4S. It is an ethyl ester derivative of thiazole-4-carboxylic acid, featuring a bromine atom and a tert-butoxycarbonylamino group. 5-BroMo-2-tert-butoxycarbonylaMino-thiazole-4-carboxylic acid ethyl ester is primarily utilized in chemical and pharmaceutical research as a versatile building block for the synthesis of other compounds. Its potential applications extend to the development of new drugs, and it may demonstrate biological activity in specific contexts. The exact properties and uses of 5-Bromo-2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester can vary depending on its application and formulation.

1279863-32-9

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1279863-32-9 Usage

Uses

Used in Chemical Research:
5-Bromo-2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester is used as a building block in chemical research for the synthesis of various compounds. Its unique structure, including the bromine atom and the tert-butoxycarbonylamino group, allows for the creation of a wide range of chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Bromo-2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester is employed as a precursor in the development of new drugs. Its potential biological activity and ability to be modified through chemical synthesis make it a valuable component in the creation of novel therapeutic agents.
Used in Drug Development:
5-Bromo-2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester is utilized in drug development as a key intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can contribute to the desired pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-Bromo-2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester is used as a starting material for the design and synthesis of new chemical entities with potential therapeutic applications. Its unique functional groups and structural features enable the exploration of various chemical modifications to optimize the drug candidates' properties.
Used in Biological Activity Studies:
5-Bromo-2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester may be used in biological activity studies to evaluate its potential effects on biological systems. Its presence in synthesized compounds can provide insights into the structure-activity relationships and contribute to the understanding of its role in various biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1279863-32-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,8,6 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1279863-32:
(9*1)+(8*2)+(7*7)+(6*9)+(5*8)+(4*6)+(3*3)+(2*3)+(1*2)=209
209 % 10 = 9
So 1279863-32-9 is a valid CAS Registry Number.

1279863-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-bromo-2-[(2-methylpropan-2-yl)oxycarbonylamino]-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names QC-6431

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:1279863-32-9 SDS

1279863-32-9Downstream Products

1279863-32-9Relevant academic research and scientific papers

COMPOUNDS AND METHODS FOR MODULATING SPLICING

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Page/Page column 167; 168, (2021/10/15)

The present disclosure features compounds and related compositions that, inter alia, modulate nucleic acid splicing, e g., splicing of a pre-mRNA, as well as methods of use thereof.

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