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1284306-63-3

(4R,5S)-4,5-dihydroxy-3-phenylcyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1284306-63-3 Structure

  • Basic information

    1. Product Name: (4R,5S)-4,5-dihydroxy-3-phenylcyclohex-2-enone
    2. Synonyms: (4R,5S)-4,5-dihydroxy-3-phenylcyclohex-2-enone
    3. CAS NO:1284306-63-3
    4. Molecular Formula:
    5. Molecular Weight: 204.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1284306-63-3.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: (4R,5S)-4,5-dihydroxy-3-phenylcyclohex-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R,5S)-4,5-dihydroxy-3-phenylcyclohex-2-enone(1284306-63-3)
    11. EPA Substance Registry System: (4R,5S)-4,5-dihydroxy-3-phenylcyclohex-2-enone(1284306-63-3)

  • 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: 1284306-63-3(Hazardous Substances Data)

1284306-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1284306-63-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,4,3,0 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1284306-63:
(9*1)+(8*2)+(7*8)+(6*4)+(5*3)+(4*0)+(3*6)+(2*6)+(1*3)=153
153 % 10 = 3
So 1284306-63-3 is a valid CAS Registry Number.

1284306-63-3Downstream Products

1284306-63-3Relevant articles and documents

Structure, stereochemistry and synthesis of enantiopure cyclohexenone cis-diol bacterial metabolites derived from phenols

Boyd, Derek R.,Sharma, Narain D.,Malone, John F.,McIntyre, Peter B. A.,Stevenson, Paul J.,Allen, Christopher C. R.,Kwit, Marcin,Gawronski, Jacek

, p. 6217 - 6229 (2012/09/05)

Biotransformation of 3-substituted and 2,5-disubstituted phenols, using whole cells of P. putida UV4, yielded cyclohexenone cis-diols as single enantiomers; their structures and absolute configurations have been determined by NMR and ECD spectroscopy, X-ray crystallography, and stereochemical correlation involving a four step chemoenzymatic synthesis from the corresponding cis-dihydrodiol metabolites. An active site model has been proposed, to account for the formation of enantiopure cyclohexenone cis-diols with opposite absolute configurations.

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