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3130-39-0

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3130-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3130-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3130-39:
(6*3)+(5*1)+(4*3)+(3*0)+(2*3)+(1*9)=50
50 % 10 = 0
So 3130-39-0 is a valid CAS Registry Number.

3130-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N6-Methyl-ATP

1.2 Other means of identification

Product number -
Other names N6-methyl-O5'-(tetrahydroxy-[1]triphosphoryl)-adenosine

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:3130-39-0 SDS

3130-39-0Upstream product

3130-39-0Downstream Products

3130-39-0Relevant articles and documents

An improved one-pot synthesis of nucleoside 5'-triphosphate analogues

Gillerman, Irina,Fischer, Bilha

, p. 245 - 256 (2010)

Nucleoside 5'-triphosphate (NTP) analogues are valuable tools for biochemical and medicinal research. Therefore, a facile and efficient synthesis of NTP analogues is required. Here, we report on an improved nucleoside 5'-triphosphorylation procedure to obtain pure products after liquid chromotagrpahy (LC) separation with no need for high performance liquid chromatography (HPLC) purification. To improve the selectivity of the reaction we attempted the optimization of several parameters such as solvent, pyrophosphate nucleophilicity, time and temperature of the reaction. Eventually, the reaction was optimized by decreasing the temperature to -15°C and increasing the reaction time to 2 hours, based on monitoring time-dependent product distribution using 31P NMR. Furthermore, the NTPs were obtained as pure products after LC separation, which was impossible in the original Ludwig procedure. Good yields were obtained for all studied natural and synthetic nucleosides.

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