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3',5'-O-bis(tert-butyldimethylsilyl)-5-([D3]methyl)-2'-deoxycytidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1245724-75-7

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1245724-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1245724-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,7,2 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1245724-75:
(9*1)+(8*2)+(7*4)+(6*5)+(5*7)+(4*2)+(3*4)+(2*7)+(1*5)=157
157 % 10 = 7
So 1245724-75-7 is a valid CAS Registry Number.

1245724-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3',5'-O-bis(tert-butyldimethylsilyl)-5-([D3]methyl)-2'-deoxycytidine

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

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

More Details:1245724-75-7 SDS

1245724-75-7Relevant academic research and scientific papers

Biomimetic Iron Complex Achieves TET Enzyme Reactivity**

Carell, Thomas,Daumann, Lena J.,Jonasson, Niko S. W.,Korytiaková, Eva,Schmidl, David

supporting information, p. 21457 - 21463 (2021/08/23)

The epigenetic marker 5-methyl-2′-deoxycytidine (5mdC) is the most prevalent modification to DNA. It is removed inter alia via an active demethylation pathway: oxidation by Ten-Eleven Translocation 5-methyl cytosine dioxygenase (TET) and subsequent removal via base excision repair or direct demodification. Recently, we have shown that the synthetic iron(IV)-oxo complex [FeIV(O)(Py5Me2H)]2+ (1) can serve as a biomimetic model for TET by oxidizing the nucleobase 5-methyl cytosine (5mC) to its natural metabolites. In this work, we demonstrate that nucleosides and even short oligonucleotide strands can also serve as substrates, using a range of HPLC and MS techniques. We found that the 5-position of 5mC is oxidized preferably by 1, with side reactions occurring only at the strand ends of the used oligonucleotides. A detailed study of the reactivity of 1 towards nucleosides confirms our results; that oxidation of the anomeric center (1′) is the most common side reaction.

Quantification of the sixth DNA base hydroxymethylcytosine in the brain

Muenzel, Martin,Globisch, Daniel,Brueckl, Tobias,Wagner, Mirko,Welzmiller, Veronika,Michalakis, Stylianos,Mueller, Markus,Biel, Martin,Carell, Thomas

supporting information; experimental part, p. 5375 - 5377 (2010/10/18)

Mind over matter: LC-MS has allowed the amount of the post-replicatively formed DNA base 5hydroxymethylcytosine (see picture; left) to be quantified in brain tissue. The nucleoside is most abundant in areas that are associated with higher cognitive functions, and its content in mouse hippocampi seems to increase with age. The new method enables hydroxymethylcytosine to be quantified with unprecedented accuracy. (Figure Presented)

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