• TCI A2900 936250-22-5 2-Aminopyrimidine-5-boronic Acid (contains varying amounts of Anhydride)
  • 936250-22-5 2-Aminopyrimidine-5-boronic Acid (contains varying amounts of Anhydride) - AMI Scientific
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TCI

CAS 936250-22-5

2-Aminopyrimidine-5-boronic Acid (contains varying amounts of Anhydride) TCI A2900

2-Aminopyrimidine-5-boronic Acid (contains varying amounts of Anhydride) TCI A2900

Chemical Identity

CAS No.
936250-22-5
PubChem
CID 17750211·SID 354334766
Formula
C4H6BN3O2
Molecular weight
138.92 g/mol
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2-aminopyrimidin-5-yl)boronic acid
SMILES
B(C1=CN=C(N=C1)N)(O)O
InChIKey
CGHYQZASLKERLV-UHFFFAOYSA-N
Rp 1.776.600,00
Rp 1.257.900,00 Rp 1.776.600,00
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2-Aminopyrimidine-5-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules and molecular modifications. It plays a crucial role in laboratory settings where precision and reactivity are essential. This compound is commonly found in coupling reactions such as the Suzuki and Heck reactions, which are fundamental in the synthesis of heterocyclic compounds and boron derivatives. As an organoboron reagent, it exhibits the ability to react with various functional groups, making it a versatile tool in organic chemistry research.

The compound's unique molecular structure, featuring both boronic acid and amino groups, contributes to its reactivity and specificity. These properties make it ideal for applications requiring high selectivity and controlled reaction conditions. The presence of varying amounts of anhydride further enhances its chemical flexibility, allowing it to adapt to different reaction environments. This adaptability makes it a valuable resource for researchers working on complex synthetic pathways.

In Indonesian laboratories, 2-Aminopyrimidine-5-boronic Acid is frequently used in organic chemistry research, especially in projects related to the synthesis of pharmacological compounds or new materials. Its reactivity and specificity make it a preferred choice for scientists aiming to achieve precise and efficient chemical transformations.

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Related TCI products

  • Organic synthesis of heterocyclic compounds due to its reactivity in coupling reactions like Suzuki and Heck.
  • Development of pharmacological compounds through precise molecular modifications in drug discovery projects.
  • Synthesis of boron-containing materials for advanced material science applications requiring functional group versatility.
  • Research in catalytic processes where organoboron reagents are essential for promoting selective chemical transformations.
  • Modification of complex molecules in synthetic chemistry, leveraging the compound's ability to interact with various functional groups.

Brand TCI
CAS number 936250-22-5
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. Due to its potential reactivity with moisture, it should be handled in a well-ventilated area. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. The compound should be kept in a secure location, away from incompatible substances to minimize the risk of chemical interactions.

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