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(5S,7R)-5,7-di[1-(tert-butyl)-1,1-dimethylsilyl]oxy-1-(4-hydroxyphenyl)icosan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 913814-44-5 Structure
  • Basic information

    1. Product Name: (5S,7R)-5,7-di[1-(tert-butyl)-1,1-dimethylsilyl]oxy-1-(4-hydroxyphenyl)icosan-3-one
    2. Synonyms: (5S,7R)-5,7-di[1-(tert-butyl)-1,1-dimethylsilyl]oxy-1-(4-hydroxyphenyl)icosan-3-one
    3. CAS NO:913814-44-5
    4. Molecular Formula:
    5. Molecular Weight: 649.158
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 913814-44-5.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: (5S,7R)-5,7-di[1-(tert-butyl)-1,1-dimethylsilyl]oxy-1-(4-hydroxyphenyl)icosan-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5S,7R)-5,7-di[1-(tert-butyl)-1,1-dimethylsilyl]oxy-1-(4-hydroxyphenyl)icosan-3-one(913814-44-5)
    11. EPA Substance Registry System: (5S,7R)-5,7-di[1-(tert-butyl)-1,1-dimethylsilyl]oxy-1-(4-hydroxyphenyl)icosan-3-one(913814-44-5)
  • 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: 913814-44-5(Hazardous Substances Data)

913814-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913814-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,8,1 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 913814-44:
(8*9)+(7*1)+(6*3)+(5*8)+(4*1)+(3*4)+(2*4)+(1*4)=165
165 % 10 = 5
So 913814-44-5 is a valid CAS Registry Number.

913814-44-5Downstream Products

913814-44-5Relevant articles and documents

Total synthesis of (+)-aculeatin D and (+)-6-epi-aculeatin D

Yadav,Raghavendra Rao,Ravindar,Subba Reddy

scheme or table, p. 51 - 54 (2010/07/10)

The stereoselective total synthesis of spiroketal natural product (+)-aculeatin D and unnatural (+)-6-epi-aculeatin D has been accomplished. Sharpless kinetic resolution of secondary allylic alcohol and phenyliodine(III) bis(trifluoroacetate) (PIFA)-mediated oxidative spirocyclization were used as key steps in this synthesis. Georg Thieme Verlag Stuttgart.

Enantioselective synthesis and absolute configurations of aculeatins A, B, D, and 6-epi-aculeatin D

álvarez-Bercedo, Paula,Falomir, Eva,Carda, Miguel,Marco

, p. 9641 - 9649 (2007/10/03)

The three naturally occurring, bioactive spiroacetals aculeatins A, B, and D, as well as the non-natural 6-epi-aculeatin D have been synthesized for the first time in enantiopure form using an asymmetric allylation as the only chirality source. A further

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