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CAS

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951037-87-9

methyl (2R)-1-((2,4,6-trimethylphenyl)sulfonyl)-2-aziridinecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 951037-87-9 Structure

  • Basic information

    1. Product Name: methyl (2R)-1-((2,4,6-trimethylphenyl)sulfonyl)-2-aziridinecarboxylate
    2. Synonyms: methyl (2R)-1-((2,4,6-trimethylphenyl)sulfonyl)-2-aziridinecarboxylate
    3. CAS NO:951037-87-9
    4. Molecular Formula:
    5. Molecular Weight: 283.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 951037-87-9.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: methyl (2R)-1-((2,4,6-trimethylphenyl)sulfonyl)-2-aziridinecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2R)-1-((2,4,6-trimethylphenyl)sulfonyl)-2-aziridinecarboxylate(951037-87-9)
    11. EPA Substance Registry System: methyl (2R)-1-((2,4,6-trimethylphenyl)sulfonyl)-2-aziridinecarboxylate(951037-87-9)

  • 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: 951037-87-9(Hazardous Substances Data)

951037-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 951037-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,0,3 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 951037-87:
(8*9)+(7*5)+(6*1)+(5*0)+(4*3)+(3*7)+(2*8)+(1*7)=169
169 % 10 = 9
So 951037-87-9 is a valid CAS Registry Number.

951037-87-9Upstream product

951037-87-9Relevant articles and documents

Versatile use of acid-catalyzed ring-opening of β-aziridinyl-α,β-enoates to stereoselective synthesis of peptidomimetics

Tamamura, Hirokazu,Tanaka, Tomohiro,Tsutsumi, Hiroshi,Nemoto, Koji,Mizokami, Satoko,Ohashi, Nami,Oishi, Shinya,Fujii, Nobutaka

, p. 9243 - 9254 (2007)

Treatment of N-arylsulfonylaziridines bearing α,β-unsaturated esters with alcohols, thiols or weak acids such as AcOH in the presence of catalytic amount of Lewis acids affords regio- and stereoselectively ring-opened products, such as δ-aminated γ-alkoxy

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