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6-Ethylamino-1,3-dimethyluracil is an organic compound with the chemical formula C7H11N3O2. It is a derivative of uracil, a pyrimidine base found in RNA, and features an ethylamine group attached to the 6-position of the uracil ring. 6-ETHYLAMINO-1,3-DIMETHYLURACIL is characterized by its white crystalline appearance and is soluble in water. It is synthesized through various chemical reactions and is used in the research and development of pharmaceuticals and other chemical applications. Due to its unique structure, 6-ethylamino-1,3-dimethyluracil has potential applications in the synthesis of novel nucleosides and as a building block for the development of new drugs targeting DNA and RNA.

5770-43-4

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5770-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5770-43-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5770-43:
(6*5)+(5*7)+(4*7)+(3*0)+(2*4)+(1*3)=104
104 % 10 = 4
So 5770-43-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H13N3O2/c1-4-9-6-5-7(12)11(3)8(13)10(6)2/h5,9H,4H2,1-3H3

5770-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(ethylamino)-1,3-dimethylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 6-Aethylamino-1,3-dimethyl-1H-pyrimidin-2,4-dion

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:5770-43-4 SDS

5770-43-4Relevant academic research and scientific papers

Selective N-Monoalkylation of 6-Aminouracils with Alcohols: An Environmentally Benign Protocol for the Synthesis of 6-Alkylaminouracils

Putra, Anggi Eka,Oe, Yohei,Ohta, Tetsuo

, p. 392 - 397 (2018/01/27)

A highly selective N-alkylation of 6-aminouracils with alcohols was achieved through the borrowing hydrogen approach using iridium catalysis. 6-Aminouracils and alcohols reacted in the presence of [Cp*IrI2]2 to give 6-monoalkyluracils selectively and in high yield (up to 99 %), usually in short reaction times (2 h). These results provide a new, green, and efficient protocol for the synthesis of 6-alkylaminouracils, which are very important intermediates for the synthesis of biologically active molecules.

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