Description
Cyclohexanecarbonyl chloride, 4-pentyl-, trans- (CAS No. 67589-90-6) is a high-purity organic compound with the molecular formula C12H21ClO. This specialized reagent is widely used in synthetic organic chemistry and pharmaceutical research due to its reactive carbonyl chloride functional group. The trans-configuration of the 4-pentylcyclohexyl moiety ensures consistent stereochemical outcomes in reactions. Offered as a clear to slightly yellow liquid, this compound is rigorously tested for purity and stability, making it ideal for sensitive applications. Proper storage under inert atmosphere and refrigeration is recommended to maintain optimal quality.
Key features include:
- High reactivity as an acylating agent
- Strict quality control for research applications
- Suitable for nucleophilic substitution reactions
- Compatible with various organic solvents
Properties
- CAS Number: 67589-90-6
- Complexity: 171
- IUPAC Name: 4-pentylcyclohexanecarbonyl chloride
- InChI: InChI=1S/C12H21ClO/c1-2-3-4-5-10-6-8-11(9-7-10)12(13)14/h10-11H,2-9H2,1H3
- InChI Key: PPWKQEDYUMJFNK-UHFFFAOYSA-N
- Exact Mass: 216.1280930
- Molecular Formula: C12H21ClO
- Molecular Weight: 216.75
- SMILES: CCCCCC1CCC(CC1)C(=O)Cl
- Topological: 17.1
- Monoisotopic Mass: 216.1280930
- Synonyms: 67589-90-6, Cyclohexanecarbonyl chloride, 4-pentyl-, trans-, Trans-4-pentylcyclohexylcarbonyl chloride, 4-PENTYLCYCLOHEXANE-1-CARBONYL CHLORIDE, SCHEMBL2576204, SCHEMBL3319559, PPWKQEDYUMJFNK-UHFFFAOYSA-N, PPWKQEDYUMJFNK-XYPYZODXSA-N, 4-n-pentylcyclohexanecarbonyl chloride, para-n-pentyl-transcyclohexanoic acid chloride, trans-4-pentylcyclohexanecarboxylic acid chloride, trans-4-n-Pentylcyclohexane-1-carboxylic acid chloride
Application
Trans-4-pentylcyclohexylcarbonyl chloride serves as a versatile building block in organic synthesis, particularly for introducing the 4-pentylcyclohexyl moiety into target molecules. It finds application in pharmaceutical intermediate synthesis, where its acyl chloride functionality enables efficient amide bond formation. Researchers utilize this compound in liquid crystal development due to its rigid cyclohexyl structure. The trans configuration makes it valuable for studying stereospecific reactions in medicinal chemistry.
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