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177905-47-4

3-Hexanone, 2-(benzoyloxy)-, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 177905-47-4 Structure

  • Basic information

    1. Product Name: 3-Hexanone, 2-(benzoyloxy)-, (2S)-
    2. Synonyms:
    3. CAS NO:177905-47-4
    4. Molecular Formula: C13H16O3
    5. Molecular Weight: 220.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177905-47-4.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: 3-Hexanone, 2-(benzoyloxy)-, (2S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Hexanone, 2-(benzoyloxy)-, (2S)-(177905-47-4)
    11. EPA Substance Registry System: 3-Hexanone, 2-(benzoyloxy)-, (2S)-(177905-47-4)

  • 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: 177905-47-4(Hazardous Substances Data)

177905-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177905-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,9,0 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 177905-47:
(8*1)+(7*7)+(6*7)+(5*9)+(4*0)+(3*5)+(2*4)+(1*7)=174
174 % 10 = 4
So 177905-47-4 is a valid CAS Registry Number.

177905-47-4Relevant articles and documents

Total synthesis of pteridic acids A and B

Paterson, Ian,Anderson, Edward A.,Findlay, Alison D.,Knappy, Christopher S.

, p. 4768 - 4777 (2008/09/20)

A convergent synthesis of pteridic acids A and B, epimeric spiroacetal polyketides with potent plant growth promoter properties, is described. The use of boron aldol methodology efficiently achieved the stereocontrolled construction of advanced C1-C11 and

Biosynthesis of tetronasin: Part 7. Preparation of structural analogues of the tetraketide biosynthetic precursor to tetronasin

Less, Simon L.,Leadlay, Peter F.,Dutton, Christopher J.,Staunton, James

, p. 3519 - 3520 (2007/10/03)

The preparation of three structural analogues of the putative tetraketide biosynthetic precursor (2) of the acyl tetronic acid ionophore tetronasin, as N-acetylcysteamine thioesters (3), (4) and (5) is described. Two examples are 19F-labelled.

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