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(R)-2,2μ-Diamino-6,6μ-dimethylbiphenyl, (R)-6,6μ-Dimethyl-2,2μ-diaminobiphenyl, (R)-6,6μ-Dimethyl-1,1μ-biphenyl-2,2μ-diamine, (R)-6,6μ-Dimethyl-1,1μ-biphenyl-2,2μ-diyldiamine CAS NO 3685-06-1
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CAS No.:3685-06-1
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
(R)-2,2μ-Diamino-6,6μ-dimethylbiphenyl, (R)-6,6μ-Dimethyl-2,2μ-diaminobiphenyl, (R)-6,6μ-Dimethyl-1,1μ-biphenyl-2,2μ-diamine, (R)-6,6μ-Dimethyl-1,1μ-biphenyl-2,2μ-diyldiamine is a high-value, chiral biphenyl diamine derivative, distinguished by its specific (R)-configuration at the stereogenic axis. This compound serves as a crucial chiral building block and ligand precursor in advanced organic synthesis and catalysis. It is primarily sought after by research institutions and industrial R&D departments in the pharmaceutical, agrochemical, and specialty chemical sectors for developing novel active ingredients and asymmetric catalysts.
Application
- Chiral Ligand Synthesis: A key precursor for the preparation of axially chiral phosphine, diamine, and N-heterocyclic carbene (NHC) ligands used in asymmetric catalysis (e.g., hydrogenation, cross-coupling).
- Pharmaceutical Intermediates: Serves as a sophisticated chiral scaffold in the synthesis of complex drug candidates, particularly those targeting central nervous system (CNS) disorders and other therapeutic areas requiring high stereochemical purity.
- Agrochemical Development: Employed in the research and production of enantiomerically pure pesticides and herbicides, where the specific stereochemistry can significantly influence biological activity and environmental safety.
- Material Science Research: Used in the development of chiral polymers, liquid crystals, and advanced organic frameworks (MOFs/COFs) with unique optical or electronic properties.
- Asymmetric Catalyst Preparation: Direct incorporation into organocatalysts or metal-complex catalysts for enantioselective transformations in fine chemical manufacturing.
- Analytical Chiral Stationary Phases: Can be utilized to develop or modify chiral stationary phases for High-Performance Liquid Chromatography (HPLC) to separate enantiomers.
Basic Information
| Item | Details |
|---|---|
| Product Name | (R)-2,2μ-Diamino-6,6μ-dimethylbiphenyl |
| CAS No. | 3685-06-1 |
| Molecular Formula | C14H16N2 |
| Molecular Weight | 212.29 g/mol |
| Synonyms | (R)-6,6μ-Dimethyl-2,2μ-diaminobiphenyl; (R)-6,6μ-Dimethyl-1,1μ-biphenyl-2,2μ-diamine; (R)-6,6μ-Dimethyl-1,1μ-biphenyl-2,2μ-diyldiamine; (R)-BINAM derivative; (R)-2,2'-Diamino-6,6'-dimethyl-1,1'-biphenyl; (R)-DMBINAM; (R)-6,6'-Dimethyl-[1,1'-biphenyl]-2,2'-diamine; (R)-Axially Chiral Diamine |
| EINECS | Contact for details |
Quality Control
Our (R)-2,2μ-Diamino-6,6μ-dimethylbiphenyl is produced under strict quality management protocols to ensure batch-to-batch consistency and high enantiomeric purity. Quality is verified through comprehensive analytical techniques including HPLC, Chiral HPLC, GC, and 1H/13C NMR. A detailed Certificate of Analysis (COA) is provided with each shipment, documenting key parameters such as assay, enantiomeric excess (ee), and impurity profiles.
Storage
Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) in a cool, dry place at 2-8°C for long-term stability. The compound is easily oxidized and light-sensitive; prolonged exposure to air, moisture, or light should be avoided to maintain purity and chiral integrity.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Purity (HPLC) | ≥ 98.0% |
| Enantiomeric Excess (Chiral HPLC) | ≥ 99.0% ee |
| Melting Point | Contact for details |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals (as Pb) | ≤ 10 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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