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8-(1-Cyclohexen-1-Ylmethyl)Theophyline CAS NO 74039-69-3


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CAS No.:74039-69-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

8-(1-Cyclohexen-1-Ylmethyl)Theophyline is a specialized xanthine derivative, structurally related to theophylline, which serves as a key intermediate in advanced pharmaceutical synthesis. This compound matters for its role in the development of novel adenosine receptor antagonists and other bioactive molecules, offering researchers and manufacturers a precise building block for drug discovery and process chemistry. It is primarily needed by pharmaceutical R&D laboratories, fine chemical producers, and academic institutions focused on developing new therapeutic agents for respiratory and neurological conditions.

Application

  • Pharmaceutical Intermediate: A critical precursor in the synthesis of novel xanthine-based drug candidates targeting adenosine receptors.
  • Research & Development: Used in academic and industrial labs for structure-activity relationship (SAR) studies and medicinal chemistry programs.
  • Fine Chemical Synthesis: Serves as a versatile building block for creating more complex heterocyclic compounds with potential biological activity.
  • Reference Standard: Employed as an analytical standard in quality control and method development for related pharmaceutical products.
  • Biochemical Research: Utilized in studies investigating the modulation of cyclic nucleotide phosphodiesterase (PDE) activity.

Basic Information

Product Name 8-(1-Cyclohexen-1-Ylmethyl)Theophyline
CAS No. 74039-69-3
Molecular Formula C₁₄H₁₈N₄O₂
Molecular Weight 274.32 g/mol
Synonyms 8-[(1-Cyclohexen-1-yl)methyl]-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione; 8-(Cyclohex-1-en-1-ylmethyl)theophylline; Theophylline, 8-[(1-cyclohexen-1-yl)methyl]-; 1,3-Dimethyl-8-((1-cyclohexen-1-yl)methyl)xanthine; 8-(Cyclohexenylmethyl)theophylline
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Quality Control

Our 8-(1-Cyclohexen-1-Ylmethyl)Theophyline is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including HPLC for assay and purity, and is supplied with a detailed Certificate of Analysis (COA). We adhere to cGMP principles for pharmaceutical intermediates, ensuring the material meets the stringent requirements for research and development applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials such as strong oxidizing agents.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.0%
Purity (HPLC) ≥ 97.0% (Total impurities ≤ 3.0%)
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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