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TCI

CAS 14036-55-6

tert-Butyl 3-Butenoate TCI B3811

tert-Butyl 3-Butenoate TCI B3811

Chemical Identity

CAS No.
14036-55-6
PubChem
CID 639778·SID 160870957
Formula
C8H14O2
Molecular weight
142.20 g/mol
Purity
>95.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl but-3-enoate
SMILES
CC(C)(C)OC(=O)CC=C
InChIKey
NGASWKRTXGWPNN-UHFFFAOYSA-N
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Tert-Butyl 3-Butenoate is a chemical compound widely used as a building block in laboratory reactions. It serves as a versatile reagent in synthetic chemistry, enabling the creation of complex molecules through various chemical transformations. This compound is commonly employed in esterification and substitution reactions, where its reactivity and stability make it an essential component in the synthesis of organic compounds. Its role in laboratory settings is critical for researchers aiming to develop new materials or pharmaceuticals.

The compound’s chemical properties make it a preferred choice for laboratory use. It is non-heterocyclic, which simplifies its integration into synthetic pathways. Its stable nature and controlled reactivity ensure predictable outcomes in chemical processes. Additionally, Tert-Butyl 3-Butenoate is odorless with a mild fragrance, making it easy to identify and handle. Its solubility in organic solvents further enhances its utility in laboratory procedures, allowing for efficient mixing and separation during experiments.

In Indonesian laboratories, Tert-Butyl 3-Butenoate is extensively used in chemical research. It is a common reagent in academic and industrial settings, supporting both basic and advanced research. Its availability and reliability make it a go-to compound for chemists working on a wide range of projects. Its consistent performance and ease of use contribute to its popularity among laboratory professionals in Indonesia.

  • Used in organic synthesis for creating complex molecular structures due to its reactivity and stability.
  • Applied in esterification reactions to form ester compounds with controlled functional groups.
  • Employed in substitution reactions to modify molecular frameworks efficiently in synthetic pathways.
  • Utilized in research for developing new pharmaceuticals and specialty chemicals through controlled chemical transformations.
  • Integrated into teaching laboratories for demonstrating fundamental chemical reactions and synthetic techniques.

Brand TCI
CAS number 14036-55-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

Tert-Butyl 3-Butenoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Suitable containers include glass or HDPE bottles with tight-fitting lids. The compound is non-hazardous under normal conditions but should be handled with care to avoid contamination. In laboratory settings, it is important to ensure proper ventilation and follow standard safety protocols when working with organic solvents. Regular inspection of storage conditions helps maintain the integrity of the compound over time.

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