Nom du produit:(5-(2-Amino-6-chloro-9H-purin-9-yl)pentyl)boronic acid
IUPAC Name:[5-(2-amino-6-chloro-9H-purin-9-yl)pentyl]boronic acid
- CAS：473870-63-2
- Formule moléculaire：C10H15BClN5O2
- Pureté：97%
- Numéro de catalogue：CM214479
- Poids moléculaire：283.52
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Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:473870-63-2
- Formule moléculaire:C10H15BClN5O2
- Point de fusion:-
- Code SMILES:ClC1=C2N=CN(CCCCCB(O)O)C2=NC(N)=N1
- Densité:
- Numéro de catalogue:CM214479
- Poids moléculaire:283.52
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Purines
- Purines are heterocyclic aromatic compounds composed of linked pyrimidine and imidazole rings. In mammals, purines are most commonly expressed in DNA and RNA (including the purines adenine and guanine), as well as single-molecule nucleotides (adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP), cyclic AMP, and to a lesser extent guanosine triphosphate (GTP) and cyclic guanosine monophosphate (cGMP). Purines are also key elements of the following energy metabolism molecules: reduced nicotinamide adenine dinucleotide, nicotinamide adenine dinucleotide phosphate (NADPH), and coenzyme Q. Purines can also act as direct neurotransmitters; for example, adenosine may interact with receptors to modulate cardiovascular and central nervous system (CNS) function.
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- Boronic Acids and Esters
- Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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- Find trusted boronic acid for sale. Any requirements and problems can ask us at any time.
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