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1,3,7,9-tetramethylpyrimido[5,4-g]pteridine-2,4,6,8(1H,3H,7H,9H)-tetrone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6439-85-6

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6439-85-6 Usage

General Description

1,3,7,9-tetramethylpyrimido[5,4-g]pteridine-2,4,6,8(1H,3H,7H,9H)-tetrone, also known as tetramethylpterin, is a chemical compound that belongs to the pteridine family. It is a yellow, crystalline substance that is insoluble in water but soluble in organic solvents. Tetramethylpterin is a precursor to several important biochemical molecules, including tetrahydrobiopterin (BH4), a cofactor in the synthesis of neurotransmitters such as serotonin, dopamine, and norepinephrine. In addition, tetramethylpterin is used as a reagent in analytical chemistry and is being investigated for its potential therapeutic applications in the treatment of various neurological and metabolic disorders. Its unique structure and biological activities make it an important molecule in both research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 6439-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6439-85:
(6*6)+(5*4)+(4*3)+(3*9)+(2*8)+(1*5)=116
116 % 10 = 6
So 6439-85-6 is a valid CAS Registry Number.

6439-85-6SDS

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 1,3,7,9-tetramethylpyrimido[5,4-g]pteridine-2,4,6,8-tetrone

1.2 Other means of identification

Product number -
Other names Pyrimido[5,4-g]pteridine-2,4,6,8(1H,3H,7H,9H)-tetrone,1,3,7,9-tetramethyl

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:6439-85-6 SDS

6439-85-6Downstream Products

6439-85-6Relevant academic research and scientific papers

5,5′-bipyridyl-2,4,6,2′,4′,6′-hexaone derivatives (hydurilic acids): Syntheses, mechanism of C-C-Bond formation and properties of the dimeric barbituric acid derivatives

Mueller, Christa E.,Roegler, Carolin,Hockemeyer, Joerg

experimental part, p. 703 - 720 (2009/12/26)

A series of hydurilic acid derivatives (5,5′-bipyrimidinyl-2,4,6,2′,4′,6′-hexaones) including several new derivatives was synthesized from 5,6-diaminouracils. Mechanisms for their formation are proposed and discussed. Furthermore, a new method for the preparation of pyrimidine-2,4,5,6-tetraone-5-oxime derivatives (violuric acids) was found starting from 5-amino-6-nitrosouracils.

A facile synthesis of pyrrolo-[3,2-d]pyrimidines from 6-azidouracils and ylide phosphoranes

Abdou, Wafaa M.,Fahmy, Amin F. M.,Kamel, Azza A.

, p. 357 - 365 (2007/10/03)

A series of the title compounds, 9-deazaxanthines, was regioselectively prepared in reasonable yields as major products from the reactions of 6-azidouracils 1a,b with stabilized ester-2a,b or keto-2c ylide phosphoranes and a moderated phosphorus ylide 3, instead of the expected triazoles. Side products were also observed wherein pyrimido[5,4-g]pteridine-2,4,5,7-tetrone (15) and other fused ring systems or acyclic-substituted uracil derivatives were isolated. A comparative study on the reactivity of 1a in analogy to 1b toward phosphoranes is also described.

A CONVERSION OF OXADIAZOLOPYRIMIDINE 1-OXIDES INTO PURINES

Yoneda, Fumio,Tachibana, Takako,Tanoue, Junko,Yano, Tetsumi,Sakuma, Yoshiharu

, p. 341 - 344 (2007/10/02)

Treatment of oxadiazolopyrimidine 1-oxides with amines led to the formation of the corresponding 8-substituted purine derivatives, along with other heterocyclic compounds in some cases.

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