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benzoyloxy-3 N-oxy methylimino-17 estra-1,3,5 (10) triene nitrone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94618-89-0 Structure
  • Basic information

    1. Product Name: benzoyloxy-3 N-oxy methylimino-17 estra-1,3,5 (10) triene nitrone
    2. Synonyms:
    3. CAS NO:94618-89-0
    4. Molecular Formula:
    5. Molecular Weight: 403.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94618-89-0.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: benzoyloxy-3 N-oxy methylimino-17 estra-1,3,5 (10) triene nitrone(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzoyloxy-3 N-oxy methylimino-17 estra-1,3,5 (10) triene nitrone(94618-89-0)
    11. EPA Substance Registry System: benzoyloxy-3 N-oxy methylimino-17 estra-1,3,5 (10) triene nitrone(94618-89-0)
  • 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: 94618-89-0(Hazardous Substances Data)

94618-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94618-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,6,1 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94618-89:
(7*9)+(6*4)+(5*6)+(4*1)+(3*8)+(2*8)+(1*9)=170
170 % 10 = 0
So 94618-89-0 is a valid CAS Registry Number.

94618-89-0Relevant articles and documents

Action de l'anhydride acetique et des chlorures de benzoyle et de p-toluene sulfonyle sur des nitrones derivees de ceto-17 steroides. Conditions conduisant a un rearrangement ou a une fonctionnalisation

Cherest, M.,Lusinchi, X.

, p. 227 - 232 (2007/10/02)

The reaction of the title reagents under anhydrous conditions and in the presence of base leads to steroidal derivatives functionalised at position 16; whereas, in the presence of water, paratoluenesulphonyl chloride gives 17-aza-D-homo lactams by ring expansion, and use of benzoyl chloride promotes a hydrolytic fragmentation.In contrast to earlier studies, the formation of an oxaziridine under aqueous alkaline conditions was not observed in this work.These results, when considered in conjunction with those previously obtained, enable the course of these reactions to be determined as a function of the reaction conditions.

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