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    Benzaldehyde
    Benzaldehyde
    Information
    CAS No. 100-52-7 Price $30 / 20mg
    Catalog No.CFN70001Purity>=98%
    Molecular Weight106.1Type of CompoundPhenols
    FormulaC7H6OPhysical DescriptionOil
    Download COA    MSDSSimilar structuralComparison
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    * Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / $7.0 / In-stock
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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    Benzaldehyde

    Benzaldehyde
    Product Name Benzaldehyde
    CAS No.: 100-52-7
    Catalog No.: CFN70001
    Molecular Formula: C7H6O
    Molecular Weight: 106.1 g/mol
    Purity: >=98%
    Type of Compound: Phenols
    Physical Desc.: Oil
    Source:
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $30 / 20mg
    Download: COA    MSDS
    Similar structural: Comparison
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  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
    Related Libraries
  • Phenols Compound Library
  • Biological Activity
    Description: Reference standards.
    Benzaldehyde Description
    Source:
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

    After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 9.4251 mL 47.1254 mL 94.2507 mL 188.5014 mL 235.6268 mL
    5 mM 1.885 mL 9.4251 mL 18.8501 mL 37.7003 mL 47.1254 mL
    10 mM 0.9425 mL 4.7125 mL 9.4251 mL 18.8501 mL 23.5627 mL
    50 mM 0.1885 mL 0.9425 mL 1.885 mL 3.77 mL 4.7125 mL
    100 mM 0.0943 mL 0.4713 mL 0.9425 mL 1.885 mL 2.3563 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    Journal of the American Chemical Society, 2008, 130(18):5854-5.
    Size-SelectiveLewis Acid Catalysis in a Microporous Metal-Organic Framework with Exposed Mn 2+ Coordination Sites.[Reference: WebLink]

    METHODS AND RESULTS:
    Treatment of selected aldehydes and ketones with cyanotrimethylsilane in the presence of the microporous metal-organic framework Mn3[(Mn4Cl)3BTT8(CH3OH)10]2 (1, H3BTT = 1,3,5-benzenetristetrazol-5-yl) leads to rapid conversion to the corresponding cyanosilylated products. The transformation is catalyzed by coordinatively unsaturated Mn2+ ions that serve as Lewis acids and lead to conversion yields of 98 and 90% for Benzaldehyde and 1-naphthaldehyde, the highest thus far for a metal-organic framework. Larger carbonyl substrates cannot diffuse through the pores of 1, and conversion yields are much lower for these, attesting to the heterogeneity of the reaction and its dependence on guest size. The Mukaiyama-aldol reaction, known to require much more active Lewis catalysts, is also catalyzed in the presence of 1, representing the first such example for a metal-organic framework. Conversion yields obtained for the reaction of selected aldehydes with silyl enolates reach 63%, on par with those obtained with zeolites.
    CONCLUSIONS:
    Size selectivity is demonstrated for the first time with this reaction through the use of larger silyl enolate substrates.
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