2-Bromothiophene TCI B0941

Chemical Identity

CAS No.: 1003-09-4
PubChem: CID 13851·SID 87563902
Formula: C4H3BrS
Molecular weight: 163.04 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromothiophene
SMILES: C1=CSC(=C1)Br
InChIKey: TUCRZHGAIRVWTI-UHFFFAOYSA-N

Rp 955.500,00

~~Rp 683.550,00~~ Rp 955.500,00

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Berat 25g 250g

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2-Bromothiophene is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. It contains both sulfur and bromine atoms, making it a versatile reagent in chemical reactions involving substitution and electrophilic processes. In laboratory settings, this compound plays a crucial role in the development of complex molecular structures necessary for pharmaceutical, material science, and organic chemistry research. Its unique chemical composition allows it to participate in various synthetic pathways, making it an essential component in the toolkit of chemists working on advanced molecular designs.

The reactivity of 2-Bromothiophene is a key factor in its popularity among researchers. The presence of bromine makes it prone to nucleophilic substitution reactions, which is highly valuable in the synthesis of complex organic molecules. Its chemical stability under controlled conditions further enhances its utility in laboratory environments. However, it is important to note that the compound is sensitive to moisture and air exposure, requiring careful handling and storage to maintain its integrity. These properties make it a preferred choice for those seeking to explore the potential of heterocyclic chemistry.

In Indonesian laboratories, 2-Bromothiophene is extensively used in scientific research related to the synthesis of heterocyclic compounds. It is a common reagent in studies focused on organic chemistry and the development of bioactive molecules. Its availability and chemical properties make it a favored material for researchers aiming to advance their work in pharmaceutical and material science fields. The compound's role in creating complex molecular structures underscores its importance in modern scientific research.

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Pharmaceutical research utilizes 2-Bromothiophene for the synthesis of bioactive compounds due to its reactivity and ability to form complex heterocyclic structures.
Organic chemistry experiments benefit from this compound as it serves as a key building block in the creation of various heterocyclic molecules.
Material science studies incorporate 2-Bromothiophene to develop new materials with unique chemical properties through heterocyclic synthesis.
Biochemistry research employs this compound in the design of molecules with potential therapeutic applications, leveraging its nucleophilic substitution capabilities.
Analytical chemistry applications use 2-Bromothiophene as a standard reference in the identification and characterization of heterocyclic compounds.

Brand	TCI
CAS number	1003-09-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from moisture and air exposure

2-Bromothiophene should be stored in a cool, dry environment to prevent degradation due to moisture and air exposure. It is recommended to use airtight containers to minimize contact with atmospheric moisture. The compound is sensitive to oxidation, so it should be handled in a controlled laboratory setting with proper ventilation. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. Storage should be in a location that is inaccessible to children and unauthorized personnel. Regular monitoring of storage conditions is essential to ensure the compound remains chemically stable and safe for use in research applications.

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