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852123-27-4

1,2-Benzenediol, 5-bromo-3-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 852123-27-4 Structure

  • Basic information

    1. Product Name: 1,2-Benzenediol, 5-bromo-3-(phenylmethoxy)-
    2. Synonyms:
    3. CAS NO:852123-27-4
    4. Molecular Formula: C13H11BrO3
    5. Molecular Weight: 295.133
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 852123-27-4.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: 1,2-Benzenediol, 5-bromo-3-(phenylmethoxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Benzenediol, 5-bromo-3-(phenylmethoxy)-(852123-27-4)
    11. EPA Substance Registry System: 1,2-Benzenediol, 5-bromo-3-(phenylmethoxy)-(852123-27-4)

  • 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: 852123-27-4(Hazardous Substances Data)

852123-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 852123-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,1,2 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 852123-27:
(8*8)+(7*5)+(6*2)+(5*1)+(4*2)+(3*3)+(2*2)+(1*7)=144
144 % 10 = 4
So 852123-27-4 is a valid CAS Registry Number.

852123-27-4Relevant articles and documents

Asymmetric synthesis of the dibenzocyclooctadiene lignans interiotherin A and gomisin R

Coleman, Robert S.,Gurrala, Srinivas Reddy

, p. 1849 - 1852 (2007/10/03)

(Chemical Equation Presented) Asymmetric total syntheses of the dibenzocyclooctadiene lignans interiotherin A and angeloylgomisin R are reported. The syntheses were based on an atropdiastereoselective, copper-promoted biaryl coupling reaction, a diastereo

Asymmetric total synthesis of dibenzocyclooctadiene lignan natural products

Coleman, Robert S.,Gurrala, Srinivas Reddy,Mitra, Soumya,Raao, Amresh

, p. 8932 - 8941 (2007/10/03)

Full details of the asymmetric total syntheses of the dibenzocyclooctadiene lignans interiotherin A, angeloylgomisin R, gomisin O, and gomisin E (epigomisin O) are presented. The syntheses were based on a unified synthetic strategy involving a novel crotylation using the Leighton auxiliary that occurred with excellent asymmetric induction (>98:2 enantiomeric ratio), a diastereoselective hydroboration/Suzuki-Miyaura coupling reaction sequence, and an atropdiastereoselective biarylcuprate coupling, both of which occurred with total (>20:1) stereocontrol. The syntheses were achieved in six to eight steps from simple aromatic precursors.

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