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CAS

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275355-92-5

(2R,4S,5S,6E)-2-benzyloxy-4,6-dimethyl-5-hydroxynon-6-en-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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  • 275355-92-5 Structure

  • Basic information

    1. Product Name: (2R,4S,5S,6E)-2-benzyloxy-4,6-dimethyl-5-hydroxynon-6-en-3-one
    2. Synonyms: (2R,4S,5S,6E)-2-benzyloxy-4,6-dimethyl-5-hydroxynon-6-en-3-one
    3. CAS NO:275355-92-5
    4. Molecular Formula:
    5. Molecular Weight: 290.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 275355-92-5.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: (2R,4S,5S,6E)-2-benzyloxy-4,6-dimethyl-5-hydroxynon-6-en-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,4S,5S,6E)-2-benzyloxy-4,6-dimethyl-5-hydroxynon-6-en-3-one(275355-92-5)
    11. EPA Substance Registry System: (2R,4S,5S,6E)-2-benzyloxy-4,6-dimethyl-5-hydroxynon-6-en-3-one(275355-92-5)

  • 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: 275355-92-5(Hazardous Substances Data)

275355-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 275355-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,5,3,5 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 275355-92:
(8*2)+(7*7)+(6*5)+(5*3)+(4*5)+(3*5)+(2*9)+(1*2)=165
165 % 10 = 5
So 275355-92-5 is a valid CAS Registry Number.

275355-92-5Relevant articles and documents

Studies in Marine Polypropionate Synthesis: Total Synthesis of (-)-Baconipyrone C

Paterson, Ian,Chen, David Yu-Kai,Acena, Jose Luis,Franklin, Alison S.

, p. 1513 - 1516 (2000)

(Equation Presented) An asymmetric total synthesis of the unusual siphonariid metabolite, (-)-baconipyrone C (3), is described. Key steps included a tin(II)-mediated aldol coupling for the preparation of the carboxylic acid 17 and two different boron-mediated aldol additions leading to alcohol 8. Ester formation using modified Yamaguchi conditions gave 24, leading on PMB deprotection to (-)-baconipyrone C.

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