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2835-45-2

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  • [5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone,5,5'-dihydroxy-1,1',3,3'-tetramethyl-

    Cas No: 2835-45-2

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2835-45-2 Usage

Description

[5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone,5,5'-dihydroxy-1,1',3,3'-tetramethylis a synthetic organic compound characterized by its complex structure, featuring a bipyrimidine core, two hydroxyl groups, and multiple methyl groups. It is classified as a ketone and is part of the broader class of compounds known as organic compounds. [5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone,5,5'-dihydroxy-1,1',3,3'-tetramethyl-'s potential applications and properties are contingent upon its reactivity, stability, and other physical and chemical attributes.

Uses

Used in Organic Synthesis:
[5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone,5,5'-dihydroxy-1,1',3,3'-tetramethylis used as a synthetic intermediate for the creation of more complex organic molecules. Its unique structure allows for various chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, dyes, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone,5,5'-dihydroxy-1,1',3,3'-tetramethylis used as a building block for the development of novel drugs. Its bipyrimidine core and functional groups may contribute to the compound's biological activity, potentially leading to the discovery of new therapeutic agents.
Used in Materials Science:
[5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone,5,5'-dihydroxy-1,1',3,3'-tetramethylmay also find applications in materials science, where its structural features could be exploited to create new materials with specific properties. These materials could be used in various applications, such as in the development of advanced polymers, sensors, or other high-tech applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2835-45-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,3 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2835-45:
(6*2)+(5*8)+(4*3)+(3*5)+(2*4)+(1*5)=92
92 % 10 = 2
So 2835-45-2 is a valid CAS Registry Number.

2835-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-5-(5-hydroxy-1,3-dimethyl-2,4,6-trioxo-1,3-diazinan-5-yl)-1,3-dimethyl-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names amalic acid

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:2835-45-2 SDS

2835-45-2Upstream product

2835-45-2Relevant articles and documents

Oxidation of nucleic acid related compounds by the peroxodisulfate ion

Itahara,Yoshitake,Koga,Nishino

, p. 2257 - 2264 (1994)

The treatment of nucleic acid bases, nucleosides, and nucleotides with peroxodisulfate ion in a phosphate buffer solution at pH 7.0 or water at 70-75°C was investigated. The reaction of thymine and 5-methylcytosine nucleosides and nucleotides resulted in the oxidation of the 5-methyl groups. The oxidation products from 1,3-dimethyluracils and the time-course of the reaction of uracils led to two plausible reaction mechanisms for the oxidation of uracils.

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