Welcome to LookChem.com Sign In|Join Free
  • or
N4-benzoyl-5'-O-benzoylcytidine is a chemical compound derived from cytidine, a nucleoside found in RNA. N4-benzoyl-5'-O-benzoylcytidine is characterized by the addition of a benzoyl group at the N4 position and a 5'-O-benzoyl group, which are both benzene-based functional groups. The N4-benzoyl group is attached to the nitrogen atom at the fourth position of the cytidine base, while the 5'-O-benzoyl group is attached to the oxygen atom at the 5' position of the ribose sugar moiety. These modifications can alter the chemical properties and interactions of the cytidine molecule, potentially affecting its stability, reactivity, or biological activity. Such derivatives are often studied in the context of drug development, as they may exhibit different pharmacological properties compared to the parent compound.

6554-15-0

Post Buying Request

6554-15-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6554-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6554-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6554-15:
(6*6)+(5*5)+(4*5)+(3*4)+(2*1)+(1*5)=100
100 % 10 = 0
So 6554-15-0 is a valid CAS Registry Number.

6554-15-0Downstream Products

6554-15-0Relevant academic research and scientific papers

Compositions and Methods for Reverse Automated Nucleic Acid Synthesis

-

Paragraph 0104-0105, (2019/10/29)

Methods for reverse automated nucleic acid synthesis, and 5′-H-phosphonates suitable for use in the same, as well as methods for making 5′-H-phosphonates, are described.

PARTIAL PROTECTION OF CARBOHYDRATE DERIVATIVES. PART 18. SIMPLE, PREPARATIVE PROCEDURE FOR 5'-O-ACYLRIBONUCLEOSIDES; HIGHLY REGIOSELECTIVE O-DEACyLATION AT 2' AND 3' POSITIONS OF FULLY ACYLATED PURINE AND PYRIMIDINE RIBONUCLEOSIDE THROUGH SODIUM METHOXYDE-THF SYSTEM

Nishino, Shigeyoshi,Rahman, MD. Azizur,Takamura, Hatsuko,Ishido, Yoshiharu

, p. 5503 - 5506 (2007/10/02)

A treatment of fully acylated purine and pyrimidine ribonucleosides with a small excess amount of sodium methoxide in THF at room temperature gave the corresponding 5'-acylates in excellent yields; N-acyl groups on the nucleic acid base moieties of adenosine and cytidine in addition to guanosine derivatives satisfactorily survived under the conditions used.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6554-15-0