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2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid is a pyrimidine-based chemical compound featuring a carboxylic acid group. It is recognized for its unique structure and reactivity, which makes it a valuable building block in medicinal chemistry for the synthesis of pharmaceuticals. The presence of both carbonyl and amino groups in the molecule allows for the formation of peptide linkages and contributes to its utility in protein synthesis.

1383056-73-2

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1383056-73-2 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid is used as a building block for the synthesis of various pharmaceuticals due to its ability to form peptide linkages and its compatibility with protein synthesis.
Used in Biochemical Research:
In the field of biochemical research, 2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid serves as a reagent, contributing to the understanding of molecular interactions and the development of new therapeutic approaches.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid is utilized for its unique reactivity, facilitating the creation of complex organic molecules and compounds.
Used in Drug Development:
2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid is used as a precursor in the development of new drugs and therapeutics, capitalizing on its structural features to explore novel medicinal properties and applications across different health-related industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1383056-73-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,0,5 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1383056-73:
(9*1)+(8*3)+(7*8)+(6*3)+(5*0)+(4*5)+(3*6)+(2*7)+(1*3)=162
162 % 10 = 2
So 1383056-73-2 is a valid CAS Registry Number.

1383056-73-2SDS

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 2-[(2-methylpropan-2-yl)oxycarbonylamino]pyrazolo[1,5-a]pyrimidine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid

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:1383056-73-2 SDS

1383056-73-2Relevant academic research and scientific papers

Substituted heteroaryl compounds and compositions and uses thereof

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Paragraph 0463-0464; 0481-0482, (2017/12/02)

The invention discloses a substituted ceteroary compound as well as a composition and an application thereof. The compound is a compound shown in a formula (I) or a stereisomer, a tautomer, a nitric oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or prodrug of the compound shown in the formula (I). The invention further discloses a pharmaceutical composition including the compound. The compound and the pharmaceutical composition are capable of adjusting the activity of the AK kinase and can be used for preventing, processing, treating and relieving the JAK-mediated disease or disorder.

SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE

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Paragraph 320, (2015/06/03)

The present invention provides novel heterocyclic compounds, pharmaceutical acceptable salts and formulations thereof useful in preventing, treating or lessening the severity of a JAK-mediated disease. The invention also provides pharmaceutically acceptable compositions comprising such compounds and methods of using the compositions in the treatment of JAK-mediated disease.

5-CHLORO-2-DIFLUOROMETHOXYPHENYL PYRAZOLOPYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF

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Paragraph 0478, (2015/12/05)

Compounds of Formula (00A) and methods of use as Janus kinase inhibitors are described herein.

PYRAZOLOPYRIMIDINE JAK INHIBITOR COMPOUNDS AND METHODS

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Page/Page column 111-112, (2011/02/24)

A compound of Formula I, enantiomers, diasteriomers, tautomers or pharmaceutically acceptable salts thereof, wherein R1, R2 and R3 are defined herein, are useful as inhibitors of one or more Janus kinases. A pharmaceutical

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