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15718-51-1

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15718-51-1 Usage

Description

CYCLIC CYTIDYLIC ACID SODIUM SALT, also known as Cytidine 2'3'-cyclic monophosphate (2',3'-Cyclic CMP) or 2',3'-cCMP, is a significant compound involved in the enzymatic synthesis of short oligoribonucleotides. It plays a crucial role in various biological processes and serves as a valuable tool for research and development in the field of molecular biology.

Uses

Used in Enzymatic Synthesis:
CYCLIC CYTIDYLIC ACID SODIUM SALT is used as a key compound in the enzymic synthesis of short oligoribonucleotides for facilitating the formation of these essential molecules in various biological processes.
Used in Research and Development:
CYCLIC CYTIDYLIC ACID SODIUM SALT is used as a model substrate for kinetic analysis of various ribonucleases, especially ribonuclease A, to study the mechanisms and properties of these enzymes in molecular biology research.
Used in Pharmaceutical Industry:
CYCLIC CYTIDYLIC ACID SODIUM SALT is used as a research tool for the development of new drugs and therapies, particularly in the areas of molecular biology and biotechnology, due to its involvement in the synthesis of oligoribonucleotides and its potential applications in gene regulation and other cellular processes.
Used in Diagnostics:
CYCLIC CYTIDYLIC ACID SODIUM SALT can be employed in the development of diagnostic tools and tests, as its interaction with ribonucleases and other enzymes can provide valuable information about the presence and activity of specific biological molecules in a sample.

Check Digit Verification of cas no

The CAS Registry Mumber 15718-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,1 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15718-51:
(7*1)+(6*5)+(5*7)+(4*1)+(3*8)+(2*5)+(1*1)=111
111 % 10 = 1
So 15718-51-1 is a valid CAS Registry Number.

15718-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name CYCLIC CYTIDYLIC ACID SODIUM SALT

1.2 Other means of identification

Product number -
Other names cytidine 2',3'-cyclic monophosphate,sodium salt

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:15718-51-1 SDS

15718-51-1Synthetic route

CYTIDINE
65-46-3

CYTIDINE

cytidine 2′,3′-cyclic monophosphate sodium salt
15718-51-1

cytidine 2′,3′-cyclic monophosphate sodium salt

Conditions
ConditionsYield
With 1H-imidazole; sodium diamido phosphate; water at 20℃; for 240h; pH=5.5;42%
cytidine-3'-monophosphate dinatrium salt

cytidine-3'-monophosphate dinatrium salt

cytidine 2′,3′-cyclic monophosphate sodium salt
15718-51-1

cytidine 2′,3′-cyclic monophosphate sodium salt

Conditions
ConditionsYield
With sodium diamido phosphate; water
C9H12N3O8P(2-)*2Na(1+)

C9H12N3O8P(2-)*2Na(1+)

cytidine 2′,3′-cyclic monophosphate sodium salt
15718-51-1

cytidine 2′,3′-cyclic monophosphate sodium salt

Conditions
ConditionsYield
With sodium diamido phosphate; water
[Ru2Cl2(N,N′‑diphenylformamidinate)3]

[Ru2Cl2(N,N′‑diphenylformamidinate)3]

cytidine 2′,3′-cyclic monophosphate sodium salt
15718-51-1

cytidine 2′,3′-cyclic monophosphate sodium salt

[Ru2Cl(N,N′‑diphenylformamidinate)3(cytidine-2′,3′-cyclic monophosphate monoanion)]

[Ru2Cl(N,N′‑diphenylformamidinate)3(cytidine-2′,3′-cyclic monophosphate monoanion)]

Conditions
ConditionsYield
In methanol at 20℃; for 25h;64%

15718-51-1Upstream product

15718-51-1Downstream Products

15718-51-1Relevant articles and documents

Phosphorylation, oligomerization and self-assembly in water under potential prebiotic conditions

Gibard, Clémentine,Bhowmik, Subhendu,Karki, Megha,Kim, Eun-Kyong,Krishnamurthy, Ramanarayanan

, p. 212 - 217 (2018/02/06)

Prebiotic phosphorylation of (pre)biological substrates under aqueous conditions is a critical step in the origins of life. Previous investigations have had limited success and/or require unique environments that are incompatible with subsequent generation of the corresponding oligomers or higher-order structures. Here, we demonstrate that diamidophosphate (DAP) - a plausible prebiotic agent produced from trimetaphosphate - efficiently (amido)phosphorylates a wide variety of (pre)biological building blocks (nucleosides/tides, amino acids and lipid precursors) under aqueous (solution/paste) conditions, without the need for a condensing agent. Significantly, higher-order structures (oligonucleotides, peptides and liposomes) are formed under the same phosphorylation reaction conditions. This plausible prebiotic phosphorylation process under similar reaction conditions could enable the systems chemistry of the three classes of (pre)biologically relevant molecules and their oligomers, in a single-pot aqueous environment.

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