CAS 35275-62-8

1-Chloro-2,3-dihydro-1H-indene

Description:

1-Chloro-2,3-dihydro-1H-indene is an organic compound characterized by its bicyclic structure, which consists of a fused indene ring system with a chlorine substituent. The presence of the chlorine atom introduces unique reactivity and properties, making it a valuable intermediate in organic synthesis. This compound typically appears as a colorless to pale yellow liquid and has a distinctive aromatic odor. Its molecular structure contributes to its moderate polarity, influencing its solubility in various organic solvents. 1-Chloro-2,3-dihydro-1H-indene is known for its potential applications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it may exhibit interesting chemical behavior, such as participating in electrophilic substitution reactions due to the electron-withdrawing nature of the chlorine atom. Safety considerations should be taken into account when handling this compound, as it may pose health risks if inhaled or ingested. Proper storage and handling protocols are essential to ensure safety in laboratory and industrial settings.

Formula: C₉H₉Cl

InChI: InChI=1S/C9H9Cl/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9H,5-6H2

InChI key: InChIKey=WLJXUWKOEVKMGD-UHFFFAOYSA-N

SMILES: ClC1C=2C(=CC=CC2)CC1

Synonyms:

• 1-Chloro-2,3-dihydroindene
• 1-Chloroindane
• 1-Indanyl chloride
• 1-chloro-2,3-dihydro-1H-indene
• 1H-Indene, 1-chloro-2,3-dihydro-
• Indan, 1-chloro-
• α-Chlorindane
• 1-Chloroindan

1-chloro-2,3-dihydro-1H-indene

CAS: 35275-62-8

Formula: C₉H₉Cl

Purity: 95%

Molecular weight: 152.6208

Ref: IN-DA00C714

1-Chloro-2,3-dihydro-1H-indene

CAS: 35275-62-8

1-Chloro-2,3-dihydro-1H-indene is a kinetic inhibitor. It has been shown to bind to the enzyme quinoline synthesis and to be reactive towards chloride ions. 1-Chloro-2,3-dihydro-1H-indene is used as an intermediate in the production of styrene. This monomer has high values for constant rate kinetics and exhibits a high affinity for chloride ions, which makes it a good candidate for use in polymerization reactions. The chlorine atom can be substituted with other atoms or groups, such as ethyl groups, halides, or transfer reactions. These derivatives are also known as quinoline derivatives.

Formula: C₉H₉Cl

Purity: Min. 95%

Molecular weight: 152.62 g/mol

Ref: 3D-KBA27562