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182616-90-6

N-((1R,2S)-1-Benzyloxymethyl-2-hydroxy-heptadecyl)-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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  • 182616-90-6 Structure

  • Basic information

    1. Product Name: N-((1R,2S)-1-Benzyloxymethyl-2-hydroxy-heptadecyl)-4-methyl-benzenesulfonamide
    2. Synonyms: N-((1R,2S)-1-Benzyloxymethyl-2-hydroxy-heptadecyl)-4-methyl-benzenesulfonamide
    3. CAS NO:182616-90-6
    4. Molecular Formula:
    5. Molecular Weight: 545.827
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182616-90-6.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-((1R,2S)-1-Benzyloxymethyl-2-hydroxy-heptadecyl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-((1R,2S)-1-Benzyloxymethyl-2-hydroxy-heptadecyl)-4-methyl-benzenesulfonamide(182616-90-6)
    11. EPA Substance Registry System: N-((1R,2S)-1-Benzyloxymethyl-2-hydroxy-heptadecyl)-4-methyl-benzenesulfonamide(182616-90-6)

  • 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: 182616-90-6(Hazardous Substances Data)

182616-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182616-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,6,1 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 182616-90:
(8*1)+(7*8)+(6*2)+(5*6)+(4*1)+(3*6)+(2*9)+(1*0)=146
146 % 10 = 6
So 182616-90-6 is a valid CAS Registry Number.

182616-90-6Relevant articles and documents

An aza-Payne rearrangement-epoxide ring opening reaction of 2-aziridinemethanols in a one-pot manner: A regio- and stereoselective synthetic route to diastereomerically pure N-protected 1,2-amino alcohols

Ibuka, Toshiro,Nakai, Kazuo,Akaji, Masako,Tamamura, Hirokazu,Fujii, Nobutaka,Yamamoto, Yoshinori

, p. 11739 - 11752 (1996)

A regio- and stereoselective synthetic route to diastereomerically pure 1,2-amino alcohols via a one-pot aza-Payne rearrangement - epoxide ring opening reaction of 2-aziridinemethanols is reported.

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