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Adenylyl(3'-5')cytidine-3'-phosphate, also known as cyclic AMP 3'-phosphate, is a cyclic nucleotide that plays a crucial role in cellular signal transduction. It is formed by the addition of a phosphate group to the 3' position of the ribose sugar in cyclic AMP (cAMP), a second messenger involved in various cellular processes. This modification enhances the stability of the molecule and can influence its interactions with target proteins, such as protein kinases, which are involved in regulating cellular activities. The presence of this chemical can affect the duration and intensity of the cellular response to external signals, making it an important component in the intricate network of cellular communication.

2348-33-6

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2348-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2348-33-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,4 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2348-33:
(6*2)+(5*3)+(4*4)+(3*8)+(2*3)+(1*3)=76
76 % 10 = 6
So 2348-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H26N8O14P2/c20-9-1-2-26(19(31)25-9)17-12(30)14(40-42(32,33)34)8(39-17)4-37-43(35,36)41-13-7(3-28)38-18(11(13)29)27-6-24-10-15(21)22-5-23-16(10)27/h1-2,5-8,11-14,17-18,28-30H,3-4H2,(H,35,36)(H2,20,25,31)(H2,21,22,23)(H2,32,33,34)/t7-,8-,11-,12-,13-,14-,17-,18-/m1/s1

2348-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methyl [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate

1.2 Other means of identification

Product number -
Other names ApCp

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:2348-33-6 SDS

2348-33-6Upstream product

2348-33-6Downstream Products

2348-33-6Relevant academic research and scientific papers

An Improved Method for the Application of the 4-Methoxybenzyl Group to Protect the 2'-Hydroxyl Group in the Ribonucleotide Synthesis by TFA-acidolysis

Losse, G.,Pechstein, Birgit

, p. 46 - 54 (2007/10/02)

The cleavage of the 4-methoxybenzyl group from the 2'-OH-position of ribonucleosides by the hydrogenation with different Pd-catalysts as well as trifluoroacetic acid has been studied in detail.During hydrogenation, side reactions at the base residue of cytidine occurred which, however, could be extensively suppressed by PdCl2 catalysis.More practicable results were obtained with trifluoroacetic acid in the presence of cation scavengers, allowing smoothly to convert a series of 2'-methoxybenzyl ribonucleotides to the homogeneous deprotection products.

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