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2,4-Di-tert-butoxypyriMidine-5-carbaldehyde is a chemical compound characterized by its molecular formula C14H21N3O3. It is a white crystalline solid that exhibits high reactivity, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structure and properties have also led to its exploration for potential biological activities, such as antifungal and antibacterial properties.

172949-72-3

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172949-72-3 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2,4-Di-tert-butoxypyriMidine-5-carbaldehyde is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its high reactivity and ability to form complex molecular structures.
Used in Organic Synthesis:
As a building block in organic synthesis, 2,4-Di-tert-butoxypyriMidine-5-carbaldehyde is employed to create a wide range of organic compounds, leveraging its reactivity to form diverse chemical entities.
Used in Biological Research:
2,4-Di-tert-butoxypyriMidine-5-carbaldehyde is utilized as a subject of study in biological research to explore its potential antifungal and antibacterial properties, which could lead to the development of new treatments or preventive measures against infections.
Used as a Reagent:
In the preparation of other organic compounds, 2,4-Di-tert-butoxypyriMidine-5-carbaldehyde serves as a reagent, contributing to the synthesis process and facilitating the creation of desired chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 172949-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,4 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 172949-72:
(8*1)+(7*7)+(6*2)+(5*9)+(4*4)+(3*9)+(2*7)+(1*2)=173
173 % 10 = 3
So 172949-72-3 is a valid CAS Registry Number.

172949-72-3SDS

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 2,4-Di-tert-butoxy-pyrimidine-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2,4-DI(TERT-BUTOXY)PYRIMIDINE-5-CARBOXALDEHYDE

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:172949-72-3 SDS

172949-72-3Downstream Products

172949-72-3Relevant academic research and scientific papers

Stereospecific synthesis of novel 1,3-thiazolidin-2-yl analogues of pseudouridine

Inaba,Inami,Kimoto,Yanada,Miwa,Taga,Bessho

, p. 1601 - 1603 (1995)

The stereospecific synthesis is described of the first member of a new class of C-nucleoside analogues in which the sugar ring is replaced with a 1,3-thiazolidine ring. The 1,3-thiazolidin-2-yl analogues (1) and (2) of pseudouridine were prepared stereospecifically via condensation of L or D- cysteine with a formylated nucleobase.

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