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CAS

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849596-51-6

(1S,3S,4S,6R,7R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-8-en-7-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 849596-51-6 Structure

  • Basic information

    1. Product Name: (1S,3S,4S,6R,7R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-8-en-7-ol
    2. Synonyms: (1S,3S,4S,6R,7R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-8-en-7-ol
    3. CAS NO:849596-51-6
    4. Molecular Formula:
    5. Molecular Weight: 308.377
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 849596-51-6.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: (1S,3S,4S,6R,7R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-8-en-7-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,3S,4S,6R,7R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-8-en-7-ol(849596-51-6)
    11. EPA Substance Registry System: (1S,3S,4S,6R,7R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-8-en-7-ol(849596-51-6)

  • 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: 849596-51-6(Hazardous Substances Data)

849596-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849596-51-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,5,9 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 849596-51:
(8*8)+(7*4)+(6*9)+(5*5)+(4*9)+(3*6)+(2*5)+(1*1)=236
236 % 10 = 6
So 849596-51-6 is a valid CAS Registry Number.

849596-51-6Relevant articles and documents

Synthesis of enantiopure cyclitols from (±)-3-bromocyclohexene mediated by intramolecular oxyselenenylation employing (S,S)-hydrobenzoin and (S)-mandelic acid as chiral sources

Lee, Yong Joo,Lee, Kyunghoon,Jung, Sea Ill,Jeon, Heung Bae,Kim, Kwan Soo

, p. 1987 - 2001 (2007/10/03)

Reaction of 3-bromocyclohexene with (S,S)-hydrobenzoin and (S)-mandelic acid and subsequent intramolecular oxyselenenylation of the resulting allylic ethers followed by oxidation-elimination afforded the valuable cis-fused bicyclic olefins, (1S,3S,4S,6R)-3,4-diphenylbicyclo[4,4,0]-2,5-dioxa-7-decene and (1S,3S,4R)-3-phenyl-4a,7,8,8a-tetrahydro-benzo[1,4]dioxan-2-one, respectively. Further stereoselective transformation of these cis-fused bicyclic olefins afforded the enantiopure cyclohexitols, muco-quercitol, D-chiro-inocitol and allo-inocitol.

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