Chemistry Heterocyclic Building Blocks Tetrahydroisoquinolines (9H-Fluoren-9-Yl)Methyl 3,4-Dihydroisoquinoline-2(1H)-Carboxylate

(9H-Fluoren-9-Yl)Methyl 3,4-Dihydroisoquinoline-2(1H)-Carboxylate

Reduction: The carbonyl group in the isoquinoline ring can be reduced to form the corresponding alcohol using reducing agents such as lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4). Hydrolysis: The ester group in the compound can undergo hydrolysis in the presence of acid or base to produce the corresponding carboxylic acid and alcohol. Esterification: The carboxylic acid group in the compound can react with alcohols in the presence of acid to form esters. Nucleophilic substitution: The compound may undergo nucleophilic substitution reactions at the carbonyl group or other reactive sites, depending on the nucleophile and reaction conditions. Oxidation: Depending on the conditions, the compound may undergo oxidation reactions, potentially leading to the formation of various oxidation products. Grignard reaction: If you have a suitable electrophilic site in the molecule, you could potentially use a Grignard reagent to form a new carbon-carbon bond. Aromatic substitution: The aromatic ring in the compound may undergo electrophilic aromatic substitution reactions if the conditions are appropriate.

Further Reading:

Framework+−

(9H-Fluoren-9-Yl)Methyl 3,4-Dihydroisoquinoline-2(1H)-Carboxylate 1,2,3,4-Tetrahydroisoquinolin-5-Amine 1,2,3,4-Tetrahydroisoquinolin-5-Ol 1,2,3,4-Tetrahydroisoquinolin-6-Amine 1,2,3,4-Tetrahydroisoquinolin-6-Ol 1,2,3,4-Tetrahydroisoquinolin-7-Amine 1,2,3,4-Tetrahydroisoquinoline-1-Carboxylic Acid 1,2,3,4-Tetrahydroisoquinoline-3-Carboxylic Acid 1,4-Dihydroisoquinolin-3(2H)-One 1-Methyl-1,2,3,4-Tetrahydroisoquinoline 2-Methyl-1,2,3,4-Tetrahydroisoquinoline 4,4-Dimethyl-1,2,3,4-Tetrahydroisoquinoline 5,6,7,8-Tetrahydroisoquinoline 5-Bromo-1,2,3,4-Tetrahydroisoquinoline 5-Chloro-1,2,3,4-Tetrahydroisoquinoline 5-Fluoro-1,2,3,4-Tetrahydroisoquinoline 5-Methyl-1,2,3,4-Tetrahydroisoquinoline 6-Bromo-1,2,3,4-Tetrahydroisoquinoline 6-Chloro-1,2,3,4-Tetrahydroisoquinoline 6-Fluoro-1,2,3,4-Tetrahydroisoquinoline 6-Methoxy-1,2,3,4-Tetrahydroisoquinoline 6-Nitro-1,2,3,4-Tetrahydroisoquinoline 7-Bromo-1,2,3,4-Tetrahydroisoquinoline 7-Chloro-1,2,3,4-Tetrahydroisoquinoline 7-Fluoro-1,2,3,4-Tetrahydroisoquinoline 7-Methoxy-1,2,3,4-Tetrahydroisoquinoline 7-Nitro-1,2,3,4-Tetrahydroisoquinoline Isoquinoline-1,3(2H,4H)-Dione

By Key Group+−

Hydroxy-Tetrahydroisoquinolin Methyl-Tetrahydroisoquinoline Other-Tetrahydroisoquinoline Phenyl-Tetrahydroisoquinoline Tetrahydroisoquinolin-Amine Tetrahydroisoquinoline-Bromide Tetrahydroisoquinoline-Carboxylate Tetrahydroisoquinoline-Carboxylic Acid Tetrahydroisoquinoline-Carboxylic-Acid Tetrahydroisoquinoline-Chloride Tetrahydroisoquinoline-Hydrochloride Tetrahydroisoquinoline-Methanol Tetrahydroisoquinoline-Nitro Trifluoromethyl-Tetrahydroisoquinoline

By Parent Nucleus+−

Aromatic Heterocycles Piperidines Pyrimidines Quinolines Spiroes Tetrahydroquinolines

By Functional Group+−

Alcohols Amides Amines Aryls Bromides Carboxylic Acids Chiral Building Blocks Chlorides Esters Ethers Fluorinated Building Blocks Ketones Nitriles Nitroes Phenols Sulfamides Trifluoromethyls

By Chemical Elements+−

    Bx
    Cx
    Nx
    Ox
    Fx
    Six
    Px
    Sx
    Clx
    Brx
    Ix

    Formula Weight+−

    cLogP+−

    H-Acceptors+−

    H-Donors+−

    Polar Surface Area+−

    Druglikeness+−

    NNCH/NNH+−

    sp3-Atoms+−

    Non-Aromatic Rings+−

    Aromatic Rings+−

    Rotatable Bonds+−

    Typically In Stock
    Purity
    • Please Select
    • 99+%
    • 99%
    • 98+%
    • 98%
    • 97+%
    • 97%
    • 96+%
    • 96%
    • 95+%
    • 95%
    • 93%
    • 90+%
    • 90%
    Size
    • Please Select
    • 1mg
    • 2mg
    • 5mg
    • 10mg
    • 25mg
    • 50mg
    • 100mg
    • 250mg
    • 1g
    • 5g
    • 10g
    • 25g
    • 100g
    • 500g
    • 1000g
    • 1kg
    Clear Filters
    2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid

    click to sign in and save

    A12632962138226-21-697%

    2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid

    $785.00/1g

    Detail
    Fmoc-(R)-2-Tetrahydroisoquinoline acetic acid

    click to sign in and save

    A673813332064-67-295%

    Fmoc-(R)-2-Tetrahydroisoquinoline acetic acid

    $150.00/1g

    Detail
    Fmoc-(S)-2-Tetrahydroisoquinoline acetic acid

    click to sign in and save

    A158036270062-99-295%

    Fmoc-(S)-2-Tetrahydroisoquinoline acetic acid

    $49.00/100mg

    Detail
    Fmoc-6-F-Tic-OH

    click to sign in and save

    A12585712197160-12-497%

    Fmoc-6-F-Tic-OH

    $442.00/250mg

    Detail
    Fmoc-D-Tic-OH

    click to sign in and save

    A151929130309-33-097%

    Fmoc-D-Tic-OH

    $61.00/25g

    Detail
    Fmoc-Tic-OH

    click to sign in and save

    A403656136030-33-698%

    Fmoc-Tic-OH

    $26.00/25g

    Detail
    2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-5-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

    click to sign in and save

    A15378712384690-34-895%

    2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-5-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

    $236.00/50mg

    Detail
    1    page 1 of 1 Pages

    Inquiry