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172949-72-3

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172949-72-3 Usage

General Description

2,4-Di-tert-butoxypyriMidine-5-carbaldehyde is a chemical compound with the molecular formula C14H21N3O3. It is a white crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2,4-Di-tert-butoxypyriMidine-5-carbaldehyde is known for its high reactivity and is often used as a building block in organic synthesis. It has also been studied for its potential biological activities, including its antifungal and antibacterial properties. Additionally, 2,4-Di-tert-butoxypyriMidine-5-carbaldehyde is used as a reagent in the preparation of other organic compounds.

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 articles and documents

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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