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CAS 206752-42-3

N6-Benzoyl-2'-deoxyadenosine Hydrate TCI B3101

N6-Benzoyl-2'-deoxyadenosine Hydrate TCI B3101

Chemical Identity

CAS No.
206752-42-3
PubChem
CID 107558·SID 87559721
Formula
C17H17N5O4
Molecular weight
355.3 g/mol
Purity
>98.0%(HPLC)(N)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N-[9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide
SMILES
C1[C@@H]([C@H](O[C@H]1N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)CO)O
InChIKey
PIXHJAPVPCVZSV-YNEHKIRRSA-N
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N6-Benzoyl-2'-deoxyadenosine Hydrate is a chemical compound widely used in biochemical and molecular biology experiments. It belongs to the nucleotide class of compounds and plays a crucial role in DNA and RNA synthesis. This compound is commonly utilized as a substrate or modification agent in studies related to nucleic acid replication and transcription mechanisms. Its presence in laboratory settings supports the development of advanced molecular techniques and biochemical research.

The compound’s chemical structure features a benzoyl group, which contributes to its reactivity and stability. These properties make it a preferred choice for controlled chemical reactions that require both stability and reactivity. The hydrate form of the compound simplifies weighing and handling in laboratory settings, ensuring consistent results during experiments. Its versatility allows it to be used in various research applications, from nucleotide modification to synthetic biology projects.

In Indonesian laboratories, N6-Benzoyl-2'-deoxyadenosine Hydrate is commonly used in molecular biology research, particularly in DNA and RNA analysis techniques. Researchers in academic and research institutions frequently employ this compound for experiments requiring nucleotide modification or the synthesis of biological compounds. Its reliability and chemical properties make it an essential tool for advancing scientific studies in the region.

  • Nucleic Acid Synthesis: This compound is ideal for synthesizing modified nucleotides, enabling the creation of custom DNA and RNA sequences for research purposes.
  • Molecular Biology Research: It supports studies on DNA replication and transcription, offering a reliable substrate for biochemical investigations.
  • Nucleotide Modification Studies: Its reactivity allows it to be used in experiments that require chemical modification of nucleotides for functional studies.
  • Biochemical Analysis: The compound is used in analytical techniques to study the behavior of nucleic acids under various experimental conditions.
  • Synthetic Biology Applications: It serves as a building block for the synthesis of complex biological molecules, aiding in the development of new therapeutic agents.

Brand TCI
CAS number 206752-42-3
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Nucleic Acid Chemistry
Pack sizes Available in various quantities as per supplier specifications
Physical form Hydrate form, typically a white or off-white solid
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is stored in a secure location, away from incompatible substances. Proper labeling of storage containers is essential to avoid mix-ups and ensure safe handling in the laboratory. Regular monitoring of storage conditions will help maintain the compound’s stability and effectiveness for research applications.

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