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CAS

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1136153-56-4

N-((1S,2S)-2-hydroxy-1,2-diphenylethyl)-2-methylpropane-2-sulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1136153-56-4 Structure

  • Basic information

    1. Product Name: N-((1S,2S)-2-hydroxy-1,2-diphenylethyl)-2-methylpropane-2-sulfonamide
    2. Synonyms: N-((1S,2S)-2-hydroxy-1,2-diphenylethyl)-2-methylpropane-2-sulfonamide
    3. CAS NO:1136153-56-4
    4. Molecular Formula:
    5. Molecular Weight: 333.452
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1136153-56-4.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: N-((1S,2S)-2-hydroxy-1,2-diphenylethyl)-2-methylpropane-2-sulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-((1S,2S)-2-hydroxy-1,2-diphenylethyl)-2-methylpropane-2-sulfonamide(1136153-56-4)
    11. EPA Substance Registry System: N-((1S,2S)-2-hydroxy-1,2-diphenylethyl)-2-methylpropane-2-sulfonamide(1136153-56-4)

  • 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: 1136153-56-4(Hazardous Substances Data)

1136153-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1136153-56-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,6,1,5 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1136153-56:
(9*1)+(8*1)+(7*3)+(6*6)+(5*1)+(4*5)+(3*3)+(2*5)+(1*6)=124
124 % 10 = 4
So 1136153-56-4 is a valid CAS Registry Number.

1136153-56-4Downstream Products

1136153-56-4Relevant articles and documents

Stereoretentive Addition of N-tert-Butylsulfonyl-α-Amido Silanes to Aldehydes, Ketones, α,β-Unsaturated Esters, and Imines

Mita, Tsuyoshi,Saito, Keisuke,Sugawara, Masumi,Sato, Yoshihiro

, p. 1528 - 1531 (2016)

Enantioenriched N-tert-butylsulfonyl-α-amido silanes were successfully reacted with aldehydes, ketones, imines, and α,β-unsaturated esters in the presence of a sub-stoichiometric amount of CsF (0.5 equiv) in 1,2-dimethoxyethane (DME) at -20 °C to afford the corresponding coupling products with up to 89 % enantiospecificity in a retentive manner. Keep your cool! Enantioenriched N-tert-butylsulfonyl-α-amido silanes were successfully reacted with aldehydes, ketones, imines, and α,β-unsaturated esters in the presence of a sub-stoichiometric amount of CsF (0.5 equiv) in 1,2-dimethoxyethane (DME) at -20 °C to afford the corresponding coupling products with up to 89 % enantiospecificity in a retentive manner.

Stereocontrolled synthesis of β-amino alcohols from lithiated aziridines and boronic esters

Schmidt, Frank,Keller, Florian,Vedrenne, Emeline,Aggarwal, Varinder K.

supporting information; experimental part, p. 1149 - 1152 (2009/06/20)

(Chemical Equation Presented) β-Amino alcohols have been prepared with high selectivity by the addition of lithiated aziridines to boronic esters. The regioselectivity of lithiation for aryl aziridines is sensitive to the reaction conditions and to the ba

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