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(S)-1-<(S)-2-Benzyl-2-methyl-2H-azirin-3-yl>-2-(1-methoxy-1-methylethyl)pyrrolidin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 171234-87-0 Structure
  • Basic information

    1. Product Name: (S)-1-<(S)-2-Benzyl-2-methyl-2H-azirin-3-yl>-2-(1-methoxy-1-methylethyl)pyrrolidin
    2. Synonyms: (S)-1-<(S)-2-Benzyl-2-methyl-2H-azirin-3-yl>-2-(1-methoxy-1-methylethyl)pyrrolidin
    3. CAS NO:171234-87-0
    4. Molecular Formula:
    5. Molecular Weight: 286.417
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 171234-87-0.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: (S)-1-<(S)-2-Benzyl-2-methyl-2H-azirin-3-yl>-2-(1-methoxy-1-methylethyl)pyrrolidin(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-<(S)-2-Benzyl-2-methyl-2H-azirin-3-yl>-2-(1-methoxy-1-methylethyl)pyrrolidin(171234-87-0)
    11. EPA Substance Registry System: (S)-1-<(S)-2-Benzyl-2-methyl-2H-azirin-3-yl>-2-(1-methoxy-1-methylethyl)pyrrolidin(171234-87-0)
  • 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: 171234-87-0(Hazardous Substances Data)

171234-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171234-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,2,3 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 171234-87:
(8*1)+(7*7)+(6*1)+(5*2)+(4*3)+(3*4)+(2*8)+(1*7)=120
120 % 10 = 0
So 171234-87-0 is a valid CAS Registry Number.

171234-87-0Relevant articles and documents

Synthesis of an enantiomerically pure 1,3-thiazole-5(4H)-thione and its stereoselective 1,3-dipolar cycloaddition with an azomethine ylide

Gebert, Andreas,Heimgartner, Heinz

, p. 2073 - 2082 (2007/10/03)

Starting from the enantiomerically pure 2H-azirin-3-amines (R,S)-4 and (S,S)-4, the enantiomeric, optically active 4-benzyl-4-methyl-2-phenyl-1,3-thiazole-5(4H)-thiones (R)-1 and (S)-1, respectively, have been prepared (Schemes 2 and 3). In each case, the

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