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Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]is a chemical compound that consists of cytidine, a nucleoside with the base cytosine attached to ribose sugar, and a sulfonyl group attached to a 2'-deoxyribose sugar. Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]is often utilized in biochemical and pharmaceutical research for studying the structure and function of nucleic acids. It may also have potential applications in the development of new drugs or therapeutic agents targeting nucleoside metabolism or nucleotide-binding enzymes. The sulfonyl group attached to the molecule may confer specific properties or reactivity, making it useful for various chemical and biological purposes. Overall, Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]is a versatile compound with potential implications in both basic research and applied sciences.

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  • 137213-26-4 Structure
  • Basic information

    1. Product Name: Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]-
    2. Synonyms:
    3. CAS NO:137213-26-4
    4. Molecular Formula: C16H19N3O6S
    5. Molecular Weight: 381.409
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137213-26-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]-(137213-26-4)
    11. EPA Substance Registry System: Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]-(137213-26-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 137213-26-4(Hazardous Substances Data)

137213-26-4 Usage

Uses

Used in Biochemical Research:
Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]is used as a research tool for studying the structure and function of nucleic acids, providing insights into their biological roles and mechanisms.
Used in Pharmaceutical Research:
Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]is used as a potential agent in the development of new drugs or therapeutic agents targeting nucleoside metabolism or nucleotide-binding enzymes, which could lead to treatments for various diseases.
Used in Chemical and Biological Applications:
The sulfonyl group in Cytidine, 2'-deoxy-N-[(4-methylphenyl)sulfonyl]may confer specific properties or reactivity to the molecule, making it useful for various chemical and biological purposes, such as the synthesis of novel compounds or the study of enzyme interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 137213-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,1 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 137213-26:
(8*1)+(7*3)+(6*7)+(5*2)+(4*1)+(3*3)+(2*2)+(1*6)=104
104 % 10 = 4
So 137213-26-4 is a valid CAS Registry Number.

137213-26-4Upstream product

137213-26-4Relevant articles and documents

Phototriggering of caged fluorescent oligodeoxynucleotides

Tang, XinJing,Dmochowski, Ivan J.

, p. 279 - 282 (2005)

(Chemical Equation Presented) We describe a synthetic route for incorporating a photocleavable (PC) DABSYL moiety and fluorescein at adjacent cytidines in the middle of a 25-mer oligodeoxynucleotide. In hybridization studies, both fluorescein and the phot

Functionalized carrier materials for the simultaneous synthesis and direct labeling of oligonucleotides as primers for template-dependent enzymatic nucleic acid syntheses

-

, (2008/06/13)

The synthesis and use of polymeric carriers is described which are loaded with nucleic acid building blocks which in turn contain labelling groups or precursors thereof. The polymeric carrier loaded in this way serves as a solid or liquid phase for the assembly of oligonucleotides which can be used as primers for template-dependent enzymatic nucleic acid syntheses such as for example in sequencing analysis according to Sanger and co-workers or in the polymerase chain reaction (PCR).

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