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2(1H)-Pyrimidinone, 4-(methylamino)(9CI), also known as cytosine N4-methyl, is a pyrimidone derivative that features a cytosine molecule with an N4-methyl substituent. This off-white solid exhibits unique chemical properties, making it a versatile compound for various applications.

6220-47-9

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6220-47-9 Usage

Uses

Used in Pharmaceutical Industry:
2(1H)-Pyrimidinone, 4-(methylamino)(9CI) is used as an active pharmaceutical ingredient for the development of drugs targeting various diseases. Its unique chemical structure allows it to interact with biological systems, making it a promising candidate for drug discovery and therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 2(1H)-Pyrimidinone, 4-(methylamino)(9CI) serves as a valuable compound for studying the properties and behavior of pyrimidone derivatives. Its unique structure provides insights into the design and synthesis of new molecules with potential applications in various industries.
Used in Biochemical Applications:
2(1H)-Pyrimidinone, 4-(methylamino)(9CI) is utilized in biochemical applications for its ability to interact with biological molecules. Its unique structure allows it to be used in the development of diagnostic tools, therapeutic agents, and other biocompatible materials.

Check Digit Verification of cas no

The CAS Registry Mumber 6220-47-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6220-47:
(6*6)+(5*2)+(4*2)+(3*0)+(2*4)+(1*7)=69
69 % 10 = 9
So 6220-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3O/c1-6-4-2-3-7-5(9)8-4/h2-3H,1H3,(H2,6,7,8,9)

6220-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N4-methylcytosine

1.2 Other means of identification

Product number -
Other names 4-methylamino-1H-pyrimidin-2-one

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:6220-47-9 SDS

6220-47-9Relevant academic research and scientific papers

A one-pot, water compatible synthesis of pyrimidine nucleobases under plausible prebiotic conditions

Okamura, Hidenori,Becker, Sidney,Tiede, Niklas,Wiedemann, Stefan,Feldmann, Jonas,Carell, Thomas

supporting information, p. 1939 - 1942 (2019/05/02)

Herein, we report a new prebiotically plausible pathway towards a pyrimidine nucleobase in continuous manner. The route involves simultaneous methylation and carbamoylation of cyanoacetylene-derived α,β-unsaturated thioamide with N-methyl-N-nitrosourea (MNU) in aqueous media. This provides S-methylpyrimidinone in one-pot, which can be converted into a variety of 4-substituted pyrimidine nucleobases including cytosine and uracil.

PHOTOCHEMICAL SYNTHESIS OF N4-SUBSTITUTED CYTOSINES

Celewicz, Lech,Spychala, Jaroslaw,Golankiewicz, Krzysztof

, p. 1939 - 1950 (2007/10/02)

The convenient method for the preparation of N4-substituted cytosines is described.The irradiation with UV light of N-(1H-2-oxo-4-pyrimidinyl)amino acids provides the proper N4-substituted cytosines in a good yield.

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