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rac-1,3-diphenylprop-2-enyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101596-62-7 Structure
  • Basic information

    1. Product Name: rac-1,3-diphenylprop-2-enyl acetate
    2. Synonyms: rac-1,3-diphenylprop-2-enyl acetate
    3. CAS NO:101596-62-7
    4. Molecular Formula:
    5. Molecular Weight: 252.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101596-62-7.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: rac-1,3-diphenylprop-2-enyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: rac-1,3-diphenylprop-2-enyl acetate(101596-62-7)
    11. EPA Substance Registry System: rac-1,3-diphenylprop-2-enyl acetate(101596-62-7)
  • 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: 101596-62-7(Hazardous Substances Data)

101596-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101596-62-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,9 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101596-62:
(8*1)+(7*0)+(6*1)+(5*5)+(4*9)+(3*6)+(2*6)+(1*2)=107
107 % 10 = 7
So 101596-62-7 is a valid CAS Registry Number.

101596-62-7Relevant articles and documents

Boron-catalyzed CC functionalization of allyl alcohols

Rao, Santhosh,Kapanaiah, Raja,Prabhu, Kandikere Ramaiah

supporting information, p. 1301 - 1306 (2019/10/28)

Tris(pentafluorophenyl)borane-catalyzed CC bond functionalization of arylallyl alcohols using donor-acceptor carbenes is presented. The allylic hydroxyl group is found to assist the product formation by neighboring group participation providing a clue towards mechanistic understanding. This method can also be employed to effect homologation of allyl alcohols to homoallyl alcohols. Overall, this metal-free transformation presents a novel disconnection strategy towards carbon-carbon bond scission and formation.

Boron-Catalyzed C?C Functionalization of Allyl Alcohols

Rao, Santhosh,Kapanaiah, Raja,Prabhu, Kandikere Ramaiah

, (2019/02/14)

Tris(pentafluorophenyl)borane-catalyzed C?C bond functionalization of arylallyl alcohols using donor-acceptor carbenes is presented. The allylic hydroxyl group is found to assist the product formation by neighboring group participation providing a clue towards mechanistic understanding. This method can also be employed to effect homologation of allyl alcohols to homoallyl alcohols. Overall, this metal-free transformation presents a novel disconnection strategy towards carbon-carbon bond scission and formation. (Figure presented.).

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