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Acetic acid (10R,13S,17S)-6-fluoro-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester is a complex organic compound with a molecular formula of C23H31FO3. It is a derivative of acetic acid, featuring a cyclopenta[a]phenanthren-17-yl ester group. Acetic acid (10R,13S,17S)-6-fluoro-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester is characterized by its unique stereochemistry, with the 10R, 13S, and 17S configurations, and the presence of a fluorine atom at the 6-position. The molecule also contains a 3-oxo group, indicating the presence of a carbonyl group, and a tetradecahydro structure, which refers to the presence of 14 hydrogen atoms in a cyclic structure. This chemical is likely to be found in specialized applications, such as pharmaceuticals or chemical research, due to its specific structural features.

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  • Acetic acid (10R,13S,17S)-6-fluoro-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester

    Cas No: 4069-09-4

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  • 4069-09-4 Structure
  • Basic information

    1. Product Name: Acetic acid (10R,13S,17S)-6-fluoro-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester
    2. Synonyms:
    3. CAS NO:4069-09-4
    4. Molecular Formula:
    5. Molecular Weight: 348.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4069-09-4.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: Acetic acid (10R,13S,17S)-6-fluoro-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid (10R,13S,17S)-6-fluoro-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester(4069-09-4)
    11. EPA Substance Registry System: Acetic acid (10R,13S,17S)-6-fluoro-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester(4069-09-4)
  • 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: 4069-09-4(Hazardous Substances Data)

4069-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4069-09-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4069-09:
(6*4)+(5*0)+(4*6)+(3*9)+(2*0)+(1*9)=84
84 % 10 = 4
So 4069-09-4 is a valid CAS Registry Number.

4069-09-4Downstream Products

4069-09-4Relevant articles and documents

Synthesis, Properties, and Reactivity of N,N'-Difluorobipyridinium and Related Salts and Their Applications as Reactive and Easy-To-Handle Electrophilic Fluorinating Agents with High Effective Fluorine Content

Umemoto, Teruo,Nagayoshi, Masayuki,Adachi, Kenji,Tomizawa, Ginjiro

, p. 3379 - 3385 (1998)

N,N′-Difluoro-2,2′-, -2,4′-, -3,3′-, -4,4′-bipyridinium and substituted N,N′-difluoro-2,2′-bipyridinmm bis(triflates), bis(tetrafluoroborates), bis(hexafluorophosphates), and bis(hexafluoroantimonates) 1-9 were synthesized in high yields by the direct fluorination of a mixture of a bipyridyl and a Lewis acid, a Br?nsted acid, or the alkali metal salt of an acid. The higher homologues, trimer 10 and polymer 11, were also synthesized. Unsubstituted or electron-donating group-substituted N,N′- difluorobipyridinium salts are stable nonhygroscopic crystals, while the electron-withdrawing group- substituted N,N′-diflurobipyridinium salts 3, 5, and 6 are moisture-sensitive crystals. Hydrolysis of 1b in boiling water gave 3,3′-dihydroxy-2,2′-bipyridyl. The reactivity determination indicated that the fluorinating capability decreased in the order 2,2′- ? 2,4' > 3,3′- ≈ 4,4′-isomer ? N-fluoropyridinium salt and that the two N-F moieties in a molecule were effective for fluorination. This fluorination occurred in a step-by-step manner, and the reactivity difference between the first and second fluorinations was very small. N,N′-Difluoro-2,2′-bipyridinium bis(tetrafluoroborate) (1b) is thus shown to be a highly reactive and easy-to-handle electrophilic fluorinating agent with the high effective fluorine content (103.3 g/kg) for preparing many fluoro organic compounds.

N-FLUOROPYRIDINIUM TRIFLATE AND ITS DERIVATES: USEFUL FLUORINATING AGENTS

Umemoto, Teruo,Kawada, Kosuke,Tomita, Kyoichi

, p. 4465 - 4468 (2007/10/02)

N-Fluoropyridinium triflate and its derivates, stable and nonhygroscopic crystals, were found to be widely applicable reagents for mild and selective fluorination of a variety of organic compounds.

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