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163399-76-6

14-Benzyloxy-tetradecan-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 163399-76-6 Structure

  • Basic information

    1. Product Name: 14-Benzyloxy-tetradecan-7-one
    2. Synonyms: 14-Benzyloxy-tetradecan-7-one
    3. CAS NO:163399-76-6
    4. Molecular Formula:
    5. Molecular Weight: 318.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 163399-76-6.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: 14-Benzyloxy-tetradecan-7-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 14-Benzyloxy-tetradecan-7-one(163399-76-6)
    11. EPA Substance Registry System: 14-Benzyloxy-tetradecan-7-one(163399-76-6)

  • 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: 163399-76-6(Hazardous Substances Data)

163399-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163399-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,3,9 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 163399-76:
(8*1)+(7*6)+(6*3)+(5*3)+(4*9)+(3*9)+(2*7)+(1*6)=166
166 % 10 = 6
So 163399-76-6 is a valid CAS Registry Number.

163399-76-6Downstream Products

163399-76-6Relevant articles and documents

Determination of the absolute configurations and total synthesis of new immunosuppressants, mycestericins E and G

Fujita, Tetsuro,Hamamichi, Norimitsu,Matsuzaki, Tohru,Kitao, Yuki,Kiuchi, Masatoshi,Node, Manabu,Hirose, Ryoji

, p. 8599 - 8602 (1995)

The absolute configurations of two new immunosuppressant, mycestericins E (1) and G (2), were established and both compounds were synthesized starting from 1,8-octanediol and a fully protected methyl (2S,4R)-oxazolidine-4-carboxylate 3. Compounds 5 and 22

Asymmetric Total Synthesis of ISP-I (Myriocin, Thermozymocidin), a Potent Immunosuppressive Principle in the Isaria sinclairii Metabolite

Shigeki, Sano,Kobayashi, Yoshimaro,Kondo, Tatsuya,Takebayashi, Maki,Maruyama, Shigeki,et al.

, p. 2097 - 2100 (2007/10/02)

Asymmetric total synthesis of ISP-I has been achived by utilizing highly selectrive E-olefin formation based on the Schlosser-modified Wittig reaction and highly diastereoselective aldol reactions employing both chiral heterocyclic derivatives, 3-acetyl-(4S)-isopropyl-1,3-thiazolidine-2-thione and ethyl -2-yl carboxylate.

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