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trans-(2R,3S)-3-(4-bromophenyl)-2-hydroxy-2,3-dihydroindan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1615249-14-3 Structure
  • Basic information

    1. Product Name: trans-(2R,3S)-3-(4-bromophenyl)-2-hydroxy-2,3-dihydroindan-1-one
    2. Synonyms:
    3. CAS NO:1615249-14-3
    4. Molecular Formula:
    5. Molecular Weight: 303.155
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1615249-14-3.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: trans-(2R,3S)-3-(4-bromophenyl)-2-hydroxy-2,3-dihydroindan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-(2R,3S)-3-(4-bromophenyl)-2-hydroxy-2,3-dihydroindan-1-one(1615249-14-3)
    11. EPA Substance Registry System: trans-(2R,3S)-3-(4-bromophenyl)-2-hydroxy-2,3-dihydroindan-1-one(1615249-14-3)
  • 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: 1615249-14-3(Hazardous Substances Data)

1615249-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1615249-14-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,5,2,4 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1615249-14:
(9*1)+(8*6)+(7*1)+(6*5)+(5*2)+(4*4)+(3*9)+(2*1)+(1*4)=153
153 % 10 = 3
So 1615249-14-3 is a valid CAS Registry Number.

1615249-14-3Upstream product

1615249-14-3Downstream Products

1615249-14-3Relevant articles and documents

Highly efficient deprotection of phenolic tetrahydropyranyl and methoxymethyl ethers and sequel cyclization to indanones using Sn(IV)Cl 4 catalyst

Ahmed, Naseem,Pathe, Gulab Khushalrao,Venkata Babu

, p. 3683 - 3687 (2014)

Sn(IV)Cl4 catalyst provided a rapid and efficient deprotection method for the phenolic THP and MOM ethers and sequel intramolecular Friedel-Crafts alkylation reaction of THP and MOM protected chalcone epoxides under mild conditions. The reaction took 2-3 min to give the products in excellent yield (90-98%) at 0 °C without affecting the other functional groups.

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