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4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene
  • 4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene

4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene

Model: 957208-65-0
The product is 4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene, a trisubstituted benzene that combines three electronically and sterically distinct functional groups: a benzylic chloromethyl moiety for nucleophilic substitution, a cyclopentyl ring that introduces saturated bulk, and a trifluoromethyl group that drastically modulates lipophilicity and metabolic stability. The 1,2,4‑substitution pattern places the chloromethyl and trifluoromethyl groups on adjacent carbon atoms, creating a unique environment where the electron‑withdrawing CF₃ group influences the reactivity of the benzylic chloride. This compound serves as a powerful alkylating agent and a key intermediate for constructing complex molecules where a rigid, fluorine‑rich aromatic ring is desired.

4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene is a specialized benzylic halide widely used in medicinal chemistry to attach a cyclopentyl‑trifluoromethylphenyl motif to nucleophilic pharmacophores. The benzylic chloride of 4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene reacts smoothly with amines, alcohols, and thiols under mild Sₙ2 conditions, allowing late‑stage diversification without affecting the trifluoromethyl or cyclopentyl groups. Because 4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene combines three distinct structural features in one building block, it enables rapid exploration of SAR around lipophilic pockets in enzyme active sites. Cosperpharm ensures that 4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene is supplied with strict control over the bis‑alkylated dimer and the corresponding benzyl alcohol, guaranteeing high conversion in subsequent N‑ or O‑alkylations.


Product Parameters

Parameter

Specification

Product Name

4-ChloroMethyl-1-cyclopentyl-2-trifluoroMethyl-benzene

CAS Number

957208-65-0

Molecular Formula

C₁₄H₁₆ClF₃

Molecular Weight

276.73 g/mol

Appearance

Colorless to pale yellow liquid

Purity (GC)

≥97.0%

Solubility

Soluble in dichloromethane, THF, toluene; insoluble in water

Storage Condition

2–8 °C, sealed under nitrogen, protect from moisture

Shelf Life

18 months under recommended conditions


Why Cosperpharm? – Our Competitive Advantages

Advantage

Detail

Production Strength

GMP-certified campus spanning 100+ mu, 3 multi-purpose workshops, 6 D-grade clean zone production lines, and 150+ reactors (20L–5000L), supporting high/low temp, anaerobic & hydrogenation; kg to ton scale production.

Fast Delivery

R&D samples: one week; commercial orders: 1–2 months after payment. Express (DHL/FedEx) or air/sea freight available.

Global Partners

Trusted by 30+ pharmaceutical companies in USA, Europe, India, Brazil, and Southeast Asia; long-term cooperation with generic drug manufacturers, CROs, and impurity standard distributors.

Licensed Exporter

Valid drug import/export license — no compliance delays.

Dual Quality Grades

Both research/pharma grade(≥98%)and high-purity impurity grade(≥99%)available to meet diverse customer needs.


Product Advantages

1.Trifluoromethyl‑Activated Benzyl Chloride – The adjacent CF₃ group enhances the electrophilicity of the chloromethyl group while blocking metabolic soft spots.

2.Saturated Cyclopentyl Ring – Introduces three‑dimensional shape and lipophilicity, often improving target selectivity over flat aromatic rings.

3.Three Orthogonal Handles – The chloride is a leaving group; the CF₃ is chemically inert; the cyclopentyl group can be further functionalized if desired.

4.Consistent Liquid Form – The low‑viscosity oil is easy to dispense by syringe or pump in both lab and kilo‑lab settings.

5.Broad Reactivity – Alkylates amines, phenols, thiophenols, and heterocycles efficiently without requiring a catalyst.


FAQ

Q: Can I use it in SₙAr reactions?

A: The chloromethyl group is an alkyl chloride; it does not participate in nucleophilic aromatic substitution. The aromatic ring is deactivated by the CF₃ group.

Q: What is the typical protocol for amine alkylation?

A: Stir the amine (1.0–1.2 equiv) with this compound in acetonitrile or DMF, using K₂CO₃ or i‑Pr₂NEt as base, at 60 °C for 4–8 h. Yields are generally >80%.


Contact Us

For a quote on this densely functionalized benzyl chloride, or to request an analytical sample for a feasibility trial, connect with Cosperpharm’s sales desk — we typically provide technical data and a pricing proposal within your preferred time frame.


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