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CAS

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129250-57-3

N-[(1R,4S)-4-(Bis-benzenesulfonyl-methyl)-cyclopent-2-enyl]-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129250-57-3 Structure

  • Basic information

    1. Product Name: N-[(1R,4S)-4-(Bis-benzenesulfonyl-methyl)-cyclopent-2-enyl]-benzamide
    2. Synonyms:
    3. CAS NO:129250-57-3
    4. Molecular Formula:
    5. Molecular Weight: 481.593
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129250-57-3.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-[(1R,4S)-4-(Bis-benzenesulfonyl-methyl)-cyclopent-2-enyl]-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(1R,4S)-4-(Bis-benzenesulfonyl-methyl)-cyclopent-2-enyl]-benzamide(129250-57-3)
    11. EPA Substance Registry System: N-[(1R,4S)-4-(Bis-benzenesulfonyl-methyl)-cyclopent-2-enyl]-benzamide(129250-57-3)

  • 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: 129250-57-3(Hazardous Substances Data)

129250-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129250-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,5 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129250-57:
(8*1)+(7*2)+(6*9)+(5*2)+(4*5)+(3*0)+(2*5)+(1*7)=123
123 % 10 = 3
So 129250-57-3 is a valid CAS Registry Number.

129250-57-3Downstream Products

129250-57-3Relevant articles and documents

Stereoselective cycloadditions of chiral acyl-nitroso compounds; synthetically useful reactions of the adducts

Miller,Procter

, p. 1043 - 1046 (1990)

The adducts from the addition of acyl-nitroso compounds do dienes are shown to undergo reactions which are important for their use in synthesis, via cleavage of the N-O bond to produce monocyclic systems followed by further functionalisation.

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