Adrenergic blocking amino alcohols and benzopyrans

dPEG4 biotin acid consists of biotin and a propionic acid-functionalized tetraethylene glycol derivative. Numerous functional or reactive groups can modify the terminal acid moiety, including the acylating agents N-hydroxysuccinimide (NHS) and

dPEG4 biotin acid consists of biotin and a propionic acid-functionalized tetraethylene glycol derivative. Numerous functional or reactive groups can modify the terminal acid moiety, including the acylating agents N-hydroxysuccinimide (NHS) and

Application This is a protected mannopyranoside useful as a building block for synthesis of complex carbohydrates. The compound has &#945-phenylthio and 6-benzyl protecting groups.

Application 1-Methylindole-2-carboxaldehyde may be used in the synthesis of indole-based melatonin analog hydrazone derivatives and ( E )-5-((benzyloxy)methyl)-5-((( tert -butyldiphenylsilyl)oxy)methyl)-3-((1-methyl-1 H

1-Phenylprop-2-en-1-one(stabilized with TBC) is an active-site directed irreversible inhibitor of hydroxynitrile lyase. Product Application:1-Phenyl-2-propen-1-one is a chemical reagent used in the synthesis of pharmaceutical agents. Used in the

1-Phenylprop-2-en-1-one(stabilized with TBC) is an active-site directed irreversible inhibitor of hydroxynitrile lyase. Product Application:1-Phenyl-2-propen-1-one is a chemical reagent used in the synthesis of pharmaceutical agents. Used in the

1-Phenylprop-2-en-1-one(stabilized with TBC) is an active-site directed irreversible inhibitor of hydroxynitrile lyase. Product Application:1-Phenyl-2-propen-1-one is a chemical reagent used in the synthesis of pharmaceutical agents. Used in the

Application 2-(Phenylthio)ethanol has been used: in the synthesis of indole, benzofuran and benzothiophene for temporary masking of the thymine residue during the synthesis of sugar modified thymidine derivatives in the preparation of

2-Aminobenzylamine undergoes three-component cyclisation reactions with methyl 3,3,3-trifluoropyruvate, 2-aminobenzylamine and oxo compounds to afford regio- and stereoisomers of tetrahydropyrroloquinazolinones. Application 2-Aminobenzylamine may

2-Aminophenethyl alcohol undergoes one-pot cyclization with carboxylic acids in the presence of PPh 3 , CCl 4 and NEt 3 to yield N -acyl indolines . Application 2-Aminophenethyl alcohol was used in the synthesis of: indole derivatives N

2H-1-Benzopyran-3-carboxamide, N-[4-(aminosulfonyl)phenyl]-2-oxo-.

2H-1-Benzopyran-3-carboxamide, N-[4-(aminosulfonyl)phenyl]-2-oxo-.