69390-84-7

Upstream product

• 100-52-7 benzaldehyde 
• 41236-20-8 3-bromopropan-1-amine hydrochloride 
• 18370-81-5 (3-bromopropyl)amine 

Downstream Products

• 67605-54-3 α-Acetylen-α,δ-diaminovaleriansaeure 
• 70052-93-6 1-benzylamino-3-bromopropane 
• 7730-39-4 N-benzyl azetidine 
• 164861-06-7 3-butyryl-4-<(2,6-dimethylphenyl)amino>-8-(3-aminopropoxy)quinoline 
• 164861-04-5 3-propanoyl-4-<(2,6-dimethylphenyl)amino>-8-(3-aminopropoxy)quinoline 
• 69730-71-8 1-iodo-3-benzaldiminopropane 
• 104739-02-8 (2S,5S)-2-<3-(benzylideneamino)propyl>-2,5-dihydro-5-isopropyl-3,6-dimethoxy-2-methylpyrazine 
• 104739-02-8 (2R,5S)-2-<3-(benzylideneamino)propyl>-2,5-dihydro-5-isopropyl-3,6-dimethoxy-2-methylpyrazine 
• 69355-11-9 hex-5-yne-1,4-diamine 

Relevant academic research and scientific papers

A facile and efficient synthesis of N-benzylazetidine

An efficient, two-step synthesis of N-benzylazetidine, starting from benzaldehyde and 3-bromopropylamine hydrobromide, is described.

N-SUBSTITUTED INDENOISOQUINOLINES AND SYNTHESES THEREOF

N-Substituted indenoisoquinoline compounds, and pharmaceutical formulations of N-substituted indenoisoquinoline compounds are described. Also described are processes for preparing N-substituted indenoisoquinoline compounds. Also described are methods for

Mechanistic considerations for the consecutive cyclization of 2,3-dibromopropylamine hydrobromide giving a strained molecule, 1-azabicyclo[1.1.0]butane

The effective formation of 1-azabicyclo[1.1.0]butane (2) by treatment of 2,3-dibromopropylamine hydrobromide (1) with n-BuLi could be understood considering a rational reaction pathway via both transition states 10 and 19 based on the intramolecular Br...

Method of inhibiting the growth of protozoa

α-Substituted amines and α-substituted-α-amino acids are described which are useful in inhibiting the growth of protozoa in animals.

Method of inhibiting algae

α-Substituted amines and α-substituted-α-amino acids are described which are useful in controlling the growth of algae.

α-Acetylenic derivatives of α-amino acids

Novel acetylenic derivatives of α-amino acids of the following general structure: STR1 wherein Z is β-methylthioethyl, β-benzylthioethyl, S-(5'-desoxyadenosin-5' -yl)-S-methylthioethyl, γ-guanidinopropyl, or RHN(CH2)n --; n is the integer 3 or 4; each R is hydrogen, alkylcarbonyl wherein the alkyl moiety has from 1 to 4 carbon atoms and is straight or branched, alkoxycarbonyl wherein the alkoxy moiety has from 1 to 4 carbon atoms and is straight or branched, or STR2 wherein R2 is hydrogen, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, benzyl or p-hydroxybenzyl; R1 is hydroxy, a straight or branched alkoxy group of from 1 to 8 carbon atoms, --NR4 R5 wherein each of R4 and R5 is hydrogen or a lower alkyl group of from 1 to 4 carbon atoms, or STR3 wherein R3 is hydrogen, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, benzyl or p-hydroxybenzyl; and the lactams thereof when Z is RHN(CH2)n -- and each R is hydrogen; with the provisos that when Z is β-benzylthioethyl or S-(5'-desoxyadenosin-5' -yl)-S-methyl-thioethyl, R is hydrogen and R1 is hydroxy, when Z is γ-guanidinopropyl, R is hydrogen and R1 is hydroxy or a straight or branched lower alkoxy group of from 1 to 8 carbon atoms, and when Z is RHN(CH2)n -- both R groups are the same; and pharmaceutically acceptable salts and individual optical isomers thereof.