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CAS

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173472-38-3

N-[(S)-1-(2-Amino-ethyl)-4-(tert-butyl-diphenyl-silanyloxy)-butyl]-4-methyl-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 173472-38-3 Structure

  • Basic information

    1. Product Name: N-[(S)-1-(2-Amino-ethyl)-4-(tert-butyl-diphenyl-silanyloxy)-butyl]-4-methyl-benzenesulfonamide
    2. Synonyms: N-[(S)-1-(2-Amino-ethyl)-4-(tert-butyl-diphenyl-silanyloxy)-butyl]-4-methyl-benzenesulfonamide
    3. CAS NO:173472-38-3
    4. Molecular Formula:
    5. Molecular Weight: 524.8
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 173472-38-3.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-[(S)-1-(2-Amino-ethyl)-4-(tert-butyl-diphenyl-silanyloxy)-butyl]-4-methyl-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(S)-1-(2-Amino-ethyl)-4-(tert-butyl-diphenyl-silanyloxy)-butyl]-4-methyl-benzenesulfonamide(173472-38-3)
    11. EPA Substance Registry System: N-[(S)-1-(2-Amino-ethyl)-4-(tert-butyl-diphenyl-silanyloxy)-butyl]-4-methyl-benzenesulfonamide(173472-38-3)

  • 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: 173472-38-3(Hazardous Substances Data)

173472-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173472-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,7 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 173472-38:
(8*1)+(7*7)+(6*3)+(5*4)+(4*7)+(3*2)+(2*3)+(1*8)=143
143 % 10 = 3
So 173472-38-3 is a valid CAS Registry Number.

173472-38-3Relevant articles and documents

The synthesis of di(hydroxyalkyl) substituted bicyclic guanidines

Madder, A.,Muenster, I.,Rolle, U.,Clercq, P. J. De

, p. 613 - 622 (2007/10/03)

The synthesis of the enantiomerically pure bicyclic guanidines 3a and 3b is described.The convergent strategy is based on methodology developed by Schmidtchen.The therefore required amine components 6 and 9 obtained from methionine and L-glutamic acid, respectively.

Synthesis of a Chiral Di(hydroxyalkyl) Substituted Bicyclic Guanidine

Muenster, Ingo,Rolle, Ulrike,Madder, Annemieke,Clerq, Pierre J. De

, p. 2673 - 2674 (2007/10/03)

Schmidtchen's methodology is used successfully for the synthesis of the chiral disubstituted bicyclic guanidinium salt 2.The two therefore required primary amine compounds 6 and 9 are obtained from L-methionine and L-glutamic acid, respectively.

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