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The chemicals mentioned are complex organic compounds with potential applications in various fields. The first compound, 2-amino-9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4,5-dihydro-1H-purin-6-one, is a derivative of purine, a heterocyclic aromatic organic compound that is a component of nucleic acids. The second compound, platinum(+2) cation, is a metal ion that can form coordination complexes with various ligands, and is known for its use in chemotherapy, particularly in the treatment of certain types of cancer. The third compound, 2-[6-(3,4,5,6-tetrahydro-2H-pyridin-2-yl)-3,4,5,6-tetrahydro-2H-pyridin-2-yl]-6H-pyridine, is a bicyclic amine with potential applications in pharmaceuticals and materials science. These compounds are characterized by their unique structures and functional groups, which confer specific properties and reactivities, making them valuable for research and development in chemistry and related disciplines.

7230-16-2

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7230-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7230-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7230-16:
(6*7)+(5*2)+(4*3)+(3*0)+(2*1)+(1*6)=72
72 % 10 = 2
So 7230-16-2 is a valid CAS Registry Number.

7230-16-2SDS

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 2-amino-9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4,5-dihydro-1H-purin-6-one,6-(6-piperidin-1-id-2-ylpiperidin-1-id-2-yl)-2H-pyridin-1-ide,platinum(2+)

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7230-16-2 SDS

7230-16-2Downstream Products

7230-16-2Relevant academic research and scientific papers

A mild, general, and metal-free method for site-specific deuteration induced by visible light using D2O as the source of deuterium atoms

Shi, Shuai,Li, Ruining,Rao, Liangming,Sun, Zhankui

supporting information, p. 669 - 672 (2020/02/21)

A radical deuteration procedure using D2O as the source of deuterium atoms is strongly preferred in terms of mildness, sustainability, and cost. Herein, we disclose a radical approach for site-specific, highly efficient and metal-free deuteration using D2O under visible light conditions. This desulfurization-deuteration strategy features mild conditions, broad substrate scope, highly efficient D-incorporation, excellent functional group compatibility, sustainable energy and is hardly affected by substrate steric factors.

Method for deuterating organic matter

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Page/Page column 5; 9; 10, (2019/10/01)

The present invention relates to a method of deuterating an organic matter, especially relates to a method of deuterating an organic compound containing a mercapto group or a disulfide bond, and belongs to the technical field of molecular marking. The method of deuterating the organic matter the following steps: dissolving the organic matter in a mixed solvent of an organic solvent and deuterium oxide, adding a phosphine reagent and a free radical initiator, and carrying out a reaction under a light condition for 3-6 h to convert the substrate into a corresponding deuterated product, wherein the organic matter is a thiol, a disulfide or a cysteine-containing polypeptide organic compound. The deuterating method has the characteristics of high deuteration efficiency, good selectivity, good functional group tolerance, high yield, mild reaction conditions, no metals participating in the reaction, wide substrate range and the like, is especially suitable for selectively deuterating the specific position of the carbon chain, and is also suitable for polypeptide substrates.

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