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Cyclohexanepropanoic acid, a-[(9-phenyl-9H-fluoren-9-yl)amino]-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 195244-97-4 Structure
  • Basic information

    1. Product Name: Cyclohexanepropanoic acid, a-[(9-phenyl-9H-fluoren-9-yl)amino]-, (S)-
    2. Synonyms:
    3. CAS NO:195244-97-4
    4. Molecular Formula: C28H29NO2
    5. Molecular Weight: 411.544
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 195244-97-4.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: Cyclohexanepropanoic acid, a-[(9-phenyl-9H-fluoren-9-yl)amino]-, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanepropanoic acid, a-[(9-phenyl-9H-fluoren-9-yl)amino]-, (S)-(195244-97-4)
    11. EPA Substance Registry System: Cyclohexanepropanoic acid, a-[(9-phenyl-9H-fluoren-9-yl)amino]-, (S)-(195244-97-4)
  • 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: 195244-97-4(Hazardous Substances Data)

195244-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195244-97-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,2,4 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 195244-97:
(8*1)+(7*9)+(6*5)+(5*2)+(4*4)+(3*4)+(2*9)+(1*7)=164
164 % 10 = 4
So 195244-97-4 is a valid CAS Registry Number.

195244-97-4Downstream Products

195244-97-4Relevant articles and documents

Enantiospecific Synthesis of N-9-Phenylfluoren-9-yl-α-amino Ketones

Paleo, M. Rita,Calaza, M. Isabel,Sardina, F. Javier

, p. 6862 - 6869 (2007/10/03)

Enantiomerically pure N-(9-phenylfluoren-9-yl)-α-amino ketones were prepared in excellent yields by acylation of organolithium reagents with N-(9-phenylfluoren-9-yl)-α-amino acid-derived oxazolidinones. The method is not applicable for the acylation of Grignard reagents as they attack the methylenic carbon of the oxazolidinone to give the corresponding N-alkylated amino acids 13 in excellent yields. The resulting N-(9-phenylfluoren-9-yl)-α-amino ketones 8 could be stereoselectively reduced to the corresponding syn- or anti-β-amino alcohols depending upon the nature of the reducing agent.

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