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C23(14)CH26F5NO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72215-98-6 Structure
  • Basic information

    1. Product Name: C23(14)CH26F5NO3
    2. Synonyms:
    3. CAS NO:72215-98-6
    4. Molecular Formula:
    5. Molecular Weight: 473.456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72215-98-6.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: C23(14)CH26F5NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23(14)CH26F5NO3(72215-98-6)
    11. EPA Substance Registry System: C23(14)CH26F5NO3(72215-98-6)
  • 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: 72215-98-6(Hazardous Substances Data)

72215-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72215-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,1 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72215-98:
(7*7)+(6*2)+(5*2)+(4*1)+(3*5)+(2*9)+(1*8)=116
116 % 10 = 6
So 72215-98-6 is a valid CAS Registry Number.

72215-98-6Upstream product

72215-98-6Downstream Products

72215-98-6Relevant articles and documents

Labelling of neuroleptic butyrophenones. II. Synthesis of 2' amino 4' fluoro 4 [4 hydroxy 4 (3 trifluoromethylphenyl)piperidino]butyrophenone (carbonyl 14C)

Nakatsuka,Kawahara,Kamada,Yoshitake

, p. 407 - 414 (1979)

2'-Amino-4'-fluoro-4-[4-hydroxy-4-(3-trifluoromethylphenyl)-piperidino]butyrophenone (1), a novel neuroleptic agent, was labelled with carbon-14 at the carbonyl position for use in metabolic studies. The synthesis was achieved according to the reaction scheme shown. Cyclopropyl 2,4-difluorophenyl ketone-(carbonyl-14C) (2a) was prepared from cyclopropane-carboxylic-14C acid by the Friedel-Crafts reaction with m-difluorobenzene. Ring-opening of 2a with hydrogen chloride gave 4-chloro-2',4'-difluorobutyrophenone-1-14C (3a). After ketalization of 3a, the resulted ketal was condensed with the piperidine and subsequently hydrolyzed with hydrochloric acid to give 6. Benzylamination of 6 with benzylamine, followed by debenzylation by catalytic hydrogenolysis gave ID-4708-(carbonyl-14C) (1). The overall radiochemical yield of 1 from barium carbonate-14C was 13%.

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