Butriptyline hydrochloride

Application 2-Butyne-1,4-diol is extensively used in the cycloaddition reactions such as the homologation method for the preparation of substituted acenes, rhodium and iridium-catalyzed [2+ 2+ 2] inter and intramolecular cyclotrimerization. It can

Application 2-Butyne-1,4-diol is extensively used in the cycloaddition reactions such as the homologation method for the preparation of substituted acenes, rhodium and iridium-catalyzed [2+ 2+ 2] inter and intramolecular cyclotrimerization. It can

Analysis Note Assay (GC, area%): &#8805 97.0 % (a/a) Melting range (lower value): &#8805 46 &#176C Melting range (upper value): &#8804 53 &#176C Identity (IR): passes test

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

3,5-Dichloroaniline

3,5-Dichloroaniline

Application 4-Butylaniline is used in the fabrication of RP/ion-exchange, mixed-mode, monolithic materials for capillary LC . Biochem/physiol Actions 4-Butylaniline is a mammalian retinoid cycle inhibitor that reversibly suppresses the recovery of

Application 4-Butylaniline is used in the fabrication of RP/ion-exchange, mixed-mode, monolithic materials for capillary LC . Biochem/physiol Actions 4-Butylaniline is a mammalian retinoid cycle inhibitor that reversibly suppresses the recovery of

Application 4-Phenyl-1-butyne can undergo addition reaction with &#945-imino esters to give the corresponding &#946,&#947-alkynyl &#945-amino acid derivatives.

4-Phenyl-3-butyn-2-one is an &#945,&#946-ketoalkyne. Reaction of 4-phenyl-3-butyn-2-one with bromine chloride and iodine monochloride in CH 2 Cl 2 , CH 2 Cl 2 /pyridine and MeOH are studied.

Synonyms: Boc-L-ß-HomoPro-OH(S)-2-(1-Boc-2-pyrrolidinyl)acetic acid(S)-2-Carboxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester Purity Limit: &ge 98% (NMR) CAS No.: 56502-01-3 Molecular Formula: C11H19NO4 Molecular Weight: 229.

cis -1,4-Dichloro-2-butene on reaction with sodium amide yields trans -1-chloro-1,3-butadiene . Mechanism of condensation of sulfone-activated methylene compounds with cis-1,4-dichloro-2-butene to yield cyclopentene has been investigated .