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Furano-Dt Cep CAS NO 858132-37-3


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CAS No.:858132-37-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Furano-Dt Cep CAS NO 858132-37-3 is a high-purity, advanced pharmaceutical intermediate belonging to the cephalosporin class of compounds. This compound is critical for the research and development of next-generation β-lactam antibiotics, offering a key structural moiety for enhancing drug efficacy and stability. It is primarily utilized by pharmaceutical R&D laboratories, fine chemical manufacturers, and academic institutions engaged in antimicrobial drug discovery and synthesis.

Application

  • Pharmaceutical Intermediate: Serves as a crucial building block in the synthetic pathway of novel cephalosporin antibiotics.
  • Antimicrobial Research: Used in academic and industrial R&D for developing new antibacterial agents with improved spectra of activity.
  • Fine Chemical Synthesis: Employed in multi-step organic syntheses to introduce the furan-fused β-lactam core structure.
  • Process Chemistry Development: Acts as a reference standard or starting material for optimizing scalable manufacturing routes for active pharmaceutical ingredients (APIs).
  • Biochemical Studies: Utilized in studies investigating the structure-activity relationship (SAR) and mechanism of action of β-lactam compounds.

Basic Information

Product Name Furano-Dt Cep
CAS No. 858132-37-3
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms (6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino]-3-[(E)-2-(furan-2-yl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; Furan-Vinyl Cephalosporin Derivative; Cefuroxime Furanyl Vinyl Analog; DT-Cep Furan; 858132-37-3
EINECS Contact for details

Quality Control

Every batch of Furano-Dt Cep is manufactured under strict quality management systems. Our products undergo rigorous quality testing, including advanced chromatographic and spectroscopic methods, to ensure compliance with research-grade and cGMP standards for pharmaceutical intermediates. Certificates of Analysis (COA) documenting purity, identity, and impurity profiles are available upon request to support your regulatory and R&D documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). This material is moisture-sensitive; keep the container tightly sealed in a dry environment.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Identification (HPLC) Conforms to reference
Purity (HPLC) ≥ 98.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.5%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Individual impurity ≤ 0.5%, Total impurities ≤ 2.0%

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

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