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1-methyl-6-(methylamino)-5-nitrosopyrimidine-2,4(1H,3H)-dione is a chemical compound with the molecular formula C6H8N4O3. It is a nitrosamine compound with a pyrimidine backbone and a nitroso group attached to the 5th carbon. The presence of a methylamino group at the 6th carbon adds to its chemical complexity.
Used in Laboratory Research:
1-methyl-6-(methylamino)-5-nitrosopyrimidine-2,4(1H,3H)-dione is used as a carcinogen and mutagen for inducing tumors in experimental animals. Its ability to cause cancer has made it a valuable tool in studying the mechanisms of carcinogenesis and developing potential cancer treatments.

29052-39-9

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29052-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29052-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,5 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29052-39:
(7*2)+(6*9)+(5*0)+(4*5)+(3*2)+(2*3)+(1*9)=109
109 % 10 = 9
So 29052-39-9 is a valid CAS Registry Number.

29052-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-6-(methylamino)-5-nitrosopyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-methyl-6-(methylamino)-5-nitrosouracil

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:29052-39-9 SDS

29052-39-9Relevant academic research and scientific papers

Purines XIV. [1]. Reactivity of 8-Bromo-3,9-dimethylxanthine Towards Some Nucleophilic Reagents

Youssef, Shaker,Pfleiderer, Wolfgang

, p. 949 - 954 (2007/10/03)

The reactivity of 8-bromo-3,9-dimethylxanthine (6) towards a variety of nucleophilic reagents has been investigated. Nucleophilic displacements take place easily with aliphatic mercaptans and aliphatic alcohols, whereas aliphatic amines required more severe conditions. Prolonged heating of 6 with amines causes a new type of rearrangement from 3,9- to 3,7-dimethylxanthines due to a 1,3-sigmatropic shift of the N(9)-methyl group.

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