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Benzenesulfonamide, 4-methyl-N-[(1R,2S)-2-methyl-1-phenyl-3-[2-(trimethylsilyl)ethoxy]propyl] - is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 877080-99-4 Structure
  • Basic information

    1. Product Name: Benzenesulfonamide, 4-methyl-N-[(1R,2S)-2-methyl-1-phenyl-3-[2-(trimethylsilyl)ethoxy]propyl] -
    2. Synonyms:
    3. CAS NO:877080-99-4
    4. Molecular Formula: C22H33NO3SSi
    5. Molecular Weight: 419.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 877080-99-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-[(1R,2S)-2-methyl-1-phenyl-3-[2-(trimethylsilyl)ethoxy]propyl] -(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-[(1R,2S)-2-methyl-1-phenyl-3-[2-(trimethylsilyl)ethoxy]propyl] -(877080-99-4)
    11. EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-[(1R,2S)-2-methyl-1-phenyl-3-[2-(trimethylsilyl)ethoxy]propyl] -(877080-99-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 877080-99-4(Hazardous Substances Data)

877080-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 877080-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,0,8 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 877080-99:
(8*8)+(7*7)+(6*7)+(5*0)+(4*8)+(3*0)+(2*9)+(1*9)=214
214 % 10 = 4
So 877080-99-4 is a valid CAS Registry Number.

877080-99-4Relevant articles and documents

Asymmetric synthesis of substituted azetidine type α- and β-amino acids

Enders, Dieter,Gries, Joerg

, p. 3508 - 3516 (2005)

A versatile asymmetric synthesis of 3-substituted azetidine-2-carboxylic acids and 2-substituted azetidine-3-carboxylic acids via 1,3-amino alcohols with excellent stereoselectivities (de ≥ 96%, ee ≥ 96%) is reported. The high asymmetric inductions were achieved employing the SAMP/RAMP-hydrazone methodology. A phenyl moiety was used as a synthetic equivalent of the carboxylic acid function. In addition, the amino acids prepared were tested as organocatalysts in an asymmetric aldol reaction. Georg Thieme Verlag Stuttgart.

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