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1186501-32-5

(S,E)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dec-1-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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  • 1186501-32-5 Structure

  • Basic information

    1. Product Name: (S,E)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dec-1-en-3-one
    2. Synonyms: (S,E)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dec-1-en-3-one
    3. CAS NO:1186501-32-5
    4. Molecular Formula:
    5. Molecular Weight: 292.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1186501-32-5.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: (S,E)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dec-1-en-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S,E)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dec-1-en-3-one(1186501-32-5)
    11. EPA Substance Registry System: (S,E)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)dec-1-en-3-one(1186501-32-5)

  • 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: 1186501-32-5(Hazardous Substances Data)

1186501-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1186501-32-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,6,5,0 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1186501-32:
(9*1)+(8*1)+(7*8)+(6*6)+(5*5)+(4*0)+(3*1)+(2*3)+(1*2)=145
145 % 10 = 5
So 1186501-32-5 is a valid CAS Registry Number.

1186501-32-5Upstream product

1186501-32-5Downstream Products

1186501-32-5Relevant articles and documents

An enantioselective synthesis of (+)-(S)-[n]-gingerols via the l-proline-catalyzed aldol reaction

Ma, Shichao,Zhang, Shilei,Duan, Wenhu,Wang, Wei

supporting information; experimental part, p. 3909 - 3911 (2010/03/25)

An enantioselective approach to (+)-(S)-[n]-gingerols (1a-c) has been developed. The requisite stereogenic centers of target molecules are facilely constructed by the proline-catalyzed cross-aldol reaction from readily available achiral starting materials

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