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Pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione, 1,3,5-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59797-09-0

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59797-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59797-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,9 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59797-09:
(7*5)+(6*9)+(5*7)+(4*9)+(3*7)+(2*0)+(1*9)=190
190 % 10 = 0
So 59797-09-0 is a valid CAS Registry Number.

59797-09-0SDS

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 1,3,5-trimethylpyrido[2,3-d]pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names pyrimidine-2,4(1H,2H)-dione

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:59797-09-0 SDS

59797-09-0Downstream Products

59797-09-0Relevant academic research and scientific papers

On the reactions of 6-phosphoranylideneaminouracils and related 6-aminouracils with 2,4,6-cyclooctatrienone: Reactions of the intermediates of uracil-annulated 8-azabicyclo[5.3.1]Undecatetraene ring systems

Nitta, Makoto,Kanda, Hiromi

, p. 491 - 499 (2007/10/03)

The reaction of 1,3-dimethyl-6-phosphoranylideneaminouracil (4) with 2,4,6-cyclooctatrienone (7) in AcOH gives an intermediacy of uracil-annulated 8-azabicyclo[5.3.1]undeca-2,4,7,9-tetraene (9), which results in the formation of 9-acetoxy-5a, 10-methano-2

SYNTHESIS OF PYRIDOPYRIMIDINE-2,4-DIONES FROM PYRIMIDO-1,2,4-TRIAZINE-6,8-DIONES BY REVERSED AZADIENE SYNTHESIS

Shorshnev, S. V.,Esipov, S. E.,Chernyshev, A. I.,Pozharskii, A. F.,Kuz'menko, V. V.,Gulevskaya, A. V.

, p. 191 - 200 (2007/10/02)

It as shown that pyrimido-1,2,4-triazine-6,8-diones enter the reversed azadiene synthesis reaction with ketones and vinyl ethyl ether in the presence of diethylamine or boron trifluoride etherate, and also with enamines.As a result of the reaction, pyridopyrimidine-2,4-diones are formed in good yield.Pyrimido-1,2,4-triazine-5,7-diones do not undergo such reactions with acetone.The reasons for the unique behavior of the isomeric pyrimidotriazinediones in the reaction with acetone are discussed.

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