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CAS 5460-29-7

N-(3-Bromopropyl)phthalimide TCI B1328

N-(3-Bromopropyl)phthalimide TCI B1328

Chemical Identity

CAS No.
5460-29-7
PubChem
CID 21611·SID 87564258
Formula
C11H10BrNO2
Molecular weight
268.11 g/mol
Purity
>98.0%(HPLC)(N)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(3-bromopropyl)isoindole-1,3-dione
SMILES
C1=CC=C2C(=C1)C(=O)N(C2=O)CCCBr
InChIKey
VKJCJJYNVIYVQR-UHFFFAOYSA-N
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N-(3-Bromopropyl)phthalimide is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It plays a crucial role in laboratory settings where the creation of heterocyclic structures or functionalized molecules is required. Its molecular structure allows for various chemical reactions, including substitution, addition, and coupling reactions, making it a versatile reagent in synthetic chemistry. This compound is particularly valuable for researchers aiming to modify molecular frameworks with high reactivity and specificity.

The compound is chemically stable under certain conditions but highly reactive in various reaction environments. This reactivity makes it a preferred choice for applications requiring high chemical activity. Its solubility in organic solvents further enhances its usability, as it simplifies handling and processing in laboratory procedures. These properties contribute to its popularity among chemists working on advanced synthetic routes and functional group transformations.

In Indonesian laboratories, N-(3-Bromopropyl)phthalimide is extensively used in organic chemistry research, especially in the development of pharmaceutical compounds and industrial chemicals. Its ability to participate in multiple reaction types and its compatibility with various synthetic strategies make it an essential component in the pursuit of complex molecular structures. Its role is particularly significant in projects involving molecular modification and functional group introduction.

  • Synthesis of Heterocyclic Compounds: This compound is ideal for creating complex ring structures due to its reactive nature and ability to undergo substitution reactions.
  • Functional Group Modification: Its brominated side chain allows for easy introduction of various functional groups, making it suitable for targeted molecular modifications.
  • Organic Synthesis in Pharmaceutical Research: It is frequently used in the development of new drug molecules due to its versatility in forming diverse chemical structures.
  • Industrial Chemical Production: The compound's reactivity and solubility make it a valuable reagent in the synthesis of specialty chemicals and intermediates.
  • Structural Elaboration in Organic Chemistry: It is used to build complex molecular frameworks, supporting research into advanced synthetic methodologies.

Brand TCI
CAS number 5460-29-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

N-(3-Bromopropyl)phthalimide should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent exposure to air and moisture. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize inhalation risks. Avoid contact with incompatible materials such as strong oxidizing agents. Always wear appropriate personal protective equipment, including gloves, safety goggles, and a lab coat, when handling this compound. Proper storage and handling practices ensure the safety of laboratory personnel and the integrity of the compound during use.

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