3-Bromobenzaldehyde Diethyl Acetal TCI B3822

Chemical Identity

CAS No.: 75148-49-1
PubChem: CID 2733543·SID 135726967
Formula: C11H15BrO2
Molecular weight: 259.14 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-bromo-3-(diethoxymethyl)benzene
SMILES: CCOC(C1=CC(=CC=C1)Br)OCC
InChIKey: KDHRJLQXMOBXRV-UHFFFAOYSA-N

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3-Bromobenzaldehyde Diethyl Acetal is a chemical compound widely used as a building block in the synthesis of complex organic molecules. This compound serves as a protected aldehyde derivative, where the aldehyde group is shielded by an acetal group, preventing unwanted side reactions during chemical processes. In the laboratory, it plays a crucial role in organic synthesis by offering a stable and reactive intermediate that can be selectively transformed into various functional groups. Its utility lies in its ability to maintain the integrity of the aldehyde functionality under controlled reaction conditions.

The compound is known for its chemical stability and reactivity under controlled environments. It exhibits non-polar characteristics, which facilitate its solubility in organic solvents such as ethyl acetate and chloroform. These properties make it an ideal choice for reactions that require the use of non-polar solvents. Additionally, its ability to resist degradation under specific chemical conditions enhances its reliability in synthetic processes. This stability ensures that the compound remains effective throughout the synthesis, contributing to the success of complex organic reactions.

In Indonesian laboratories, 3-Bromobenzaldehyde Diethyl Acetal is extensively used in organic chemistry research, particularly in the synthesis of heterocyclic and aromatic compounds. Its availability and consistent performance make it a valuable resource for both academic and industrial research. It is commonly employed in the development of new chemical compounds and pharmaceutical intermediates, supporting advancements in chemical innovation and scientific discovery.

Related TCI products

Organic synthesis of heterocyclic compounds due to its protected aldehyde functionality and reactivity in controlled environments.
Preparation of aromatic derivatives through selective chemical transformations under laboratory conditions.
Development of pharmaceutical intermediates where stability and controlled reactivity are essential.
Research in chemical innovation requiring reliable and stable building blocks for complex molecule synthesis.
Use in academic and industrial research settings for the advancement of chemical processes and material development.

Brand	TCI
CAS number	75148-49-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible substances

This compound should be stored in a cool, dry location, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its non-polar nature, it is important to ensure proper ventilation in the laboratory when handling this material. Avoid contact with incompatible substances such as strong oxidizers or acids. Always follow standard laboratory safety protocols, including the use of personal protective equipment when handling or storing this compound. Proper storage ensures the compound remains stable and effective for use in chemical synthesis processes.

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