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3-(2-bromophenyl)-1-(pyridin-2-yl)propan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1378939-14-0 Structure
  • Basic information

    1. Product Name: 3-(2-bromophenyl)-1-(pyridin-2-yl)propan-1-ol
    2. Synonyms:
    3. CAS NO:1378939-14-0
    4. Molecular Formula:
    5. Molecular Weight: 292.175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1378939-14-0.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: 3-(2-bromophenyl)-1-(pyridin-2-yl)propan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-bromophenyl)-1-(pyridin-2-yl)propan-1-ol(1378939-14-0)
    11. EPA Substance Registry System: 3-(2-bromophenyl)-1-(pyridin-2-yl)propan-1-ol(1378939-14-0)
  • 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: 1378939-14-0(Hazardous Substances Data)

1378939-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1378939-14-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,8,9,3 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1378939-14:
(9*1)+(8*3)+(7*7)+(6*8)+(5*9)+(4*3)+(3*9)+(2*1)+(1*4)=220
220 % 10 = 0
So 1378939-14-0 is a valid CAS Registry Number.

1378939-14-0Downstream Products

1378939-14-0Relevant articles and documents

Synthesis of 2-aryl-substituted chromans by intramolecular C-O bond formation

Wang, Yu,Franzén, Robert

, p. 925 - 929 (2012/06/15)

A synthetic route for the preparation of 2-aryl-substituted chromans from commercially available starting materials and utilizing either a palladium- or copper-catalyzed intramolecular cyclization of aryl bromides is described. Chromans with stereocontrol at C-2 can thus be obtained via a palladium-catalyzed asymmetric allylic etherification procedure utilizing a chiral indole-phosphine oxazoline (IndPHOX) ligand. Georg Thieme Verlag Stuttgart · New York.

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