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TCI

CAS 10293-06-8

(+)-3-Bromocamphor TCI B0567

(+)-3-Bromocamphor TCI B0567

Chemical Identity

CAS No.
10293-06-8
PubChem
CID 44630109·SID 87563585
Formula
C10H15BrO
Molecular weight
231.13 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(3S,4S)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
SMILES
CC1([C@@H]2CCC1(C(=O)[C@H]2Br)C)C
InChIKey
NJQADTYRAYFBJN-MZVBAPTMSA-N
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(+)-3-Bromocamphor is a chiral building block widely used in asymmetric synthesis to produce compounds with specific stereochemical configurations. This compound plays a crucial role in organic chemistry laboratories where precise control over molecular structure is essential. Its chiral nature allows it to serve as a key intermediate in the synthesis of optically active compounds, making it indispensable in research focused on enantioselective reactions. Due to its unique molecular structure, it is frequently utilized in advanced chemical synthesis processes that require high precision and specificity.

One of the main reasons (+)-3-Bromocamphor is preferred is its stable molecular framework, which ensures consistent performance in various chemical reactions. Its ability to participate in reactions that demand specific reactivity makes it a versatile tool for chemists. Additionally, the compound exhibits favorable physical properties that simplify handling, storage, and integration into laboratory workflows. These characteristics contribute to its popularity among researchers working on complex organic synthesis projects.

In Indonesian laboratories, (+)-3-Bromocamphor is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of new compounds. It is a go-to material for scientists in academic and research institutions who require precise control over stereochemistry. Its application in these settings highlights its importance in advancing chemical research and innovation in the region.

TCI brochures (PDF)

  • Asymmetric Synthesis: This compound is ideal for creating chiral molecules with specific stereochemistry, enabling precise control over reaction outcomes in complex organic syntheses.
  • Chiral Compound Development: Its chiral structure makes it a valuable resource for developing new optically active compounds used in pharmaceutical and material sciences.
  • Organic Chemistry Research: It is widely used in laboratories for studying reaction mechanisms and exploring new synthetic pathways involving chiral intermediates.
  • Pharmaceutical Research: Its role in synthesizing bioactive molecules makes it a key component in drug discovery and development processes.
  • Academic Teaching: It is frequently used in educational settings to demonstrate the principles of stereochemistry and asymmetric synthesis to students.

Brand TCI
CAS number 10293-06-8
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

(+)-3-Bromocamphor should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its stability. Avoid direct sunlight and high humidity conditions to ensure optimal preservation. In laboratory settings, proper ventilation should be maintained when handling the compound to minimize inhalation risks. Always use appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. Ensure that storage areas are secure and inaccessible to unauthorized personnel to maintain safety standards.

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