116784-97-5

Usage

Uses

Used in Pharmaceutical Synthesis:
(6-BROMO-HEXYL)-CARBAMIC ACID BENZYL ESTER is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows it to be a key component in the development of new medications, contributing to the advancement of healthcare.
Used in Agrochemical Production:
In the agrochemical industry, (6-BROMO-HEXYL)-CARBAMIC ACID BENZYL ESTER is utilized as an intermediate in the production of various agrochemicals. Its role in this sector is crucial for the development of effective and safe products for agricultural use.
Used in Organic Compound Production:
(6-BROMO-HEXYL)-CARBAMIC ACID BENZYL ESTER is used as a precursor in the synthesis of organic compounds. Its versatility in chemical reactions makes it a valuable component in the creation of a wide range of organic molecules.
Used in Chemical Research:
In the field of chemical research, (6-BROMO-HEXYL)-CARBAMIC ACID BENZYL ESTER is employed as a research compound. Its unique properties and reactivity make it an important tool for scientists to study and understand various chemical processes and reactions.
It is important to handle (6-BROMO-HEXYL)-CARBAMIC ACID BENZYL ESTER with care, as it can be harmful if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken during its use to ensure the well-being of individuals and the environment.

InChI:InChI=1/C14H20BrNO2/c15-10-6-1-2-7-11-16-14(17)18-12-13-8-4-3-5-9-13/h3-5,8-9H,1-2,6-7,10-12H2,(H,16,17)

Upstream product

• 14502-76-2 6-bromo-1-aminohexane hydrobromide 
• 501-53-1 benzyl chloroformate 
• 17996-12-2 N-benzyloxycarbonyl-6-amino-1-hexanol 
• 4048-33-3 6-amino-1-hexanol 

Downstream Products

• 116784-98-6 N-<(benzyloxy)carbonyl>-N'-methyl-1,6-hexanediamine 
• 528840-32-6 4,7-N,N-di-tert-butyloxycarbonyl-1-N-[6-(N-benzyloxycarbonyl)aminohexyl]-1,4,7-triazacyclononane 
• 906672-26-2 [6-(2-hydroxy(tripolyethyleneglycol)hexyl)]carbamic acid benzyl ester 
• 957829-63-9 10-(6-benzyloxycarbonylamino-hexyl)-1,4,7,10-tetraaza-cyclododecane-1,4,7-tricarboxylic acid tri-tert-butyl ester 
• 912757-86-9 C₂₄H₃₃N₃O₇ 
• 51224-11-4 6-(benzyloxycarbonylamino)-1-iodohexane 
• 116784-99-7 N-<(benzyloxy)carbonyl>-N'-(2-furoyl)-N'-methyl-1,6-hexanediamine 
• 688790-72-9 9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid [6-(cis-3,5-(N,N-di-tert-butyloxycarbonyl)diaminocyclohexylamino)hexyl]amide 
• 688790-69-4 all-cis-3,5-N,N-di-tert-butyloxycarbonyl-1-N-(6-aminohexyl)-1,3,5-triaminocyclohexane 
• 688790-66-1 all-cis-3,5-N,N-di-tert-butyloxycarbonyl-1-N-[6-N-(benzyloxycarbonyl)aminohexyl]-1,3,5-triaminocyclohexane 

Relevant academic research and scientific papers

Glycerophosphoinositols: Total synthesis of the first fluorescent probe derivative

The first fluorescent glycerophosphoinositol probe was synthesized in moderate good yield (37%). The total synthesis applied a convergent synthetic strategy involving two successive coupling reactions between the three key moieties: myo-inositol, glycerol

Poly(ethylene glycol)-supported copper(II) triazacyclononane: An efficient, recoverable, and recyclable catalyst for the cleavage of a phosphodiester

The triazacyclononane macrocycle has been linked to the soluble polymer monomethoxy poly(ethylene) glycol and its copper(II) complex efficiently catalyzes the hydrolysis of a model phosphodiester. The catalyst, easily recovered from the water solution, sh

Regio- and chemoselective covalent immobilization of proteins through unnatural amino acids

A general approach was developed for the regio- and chemoselective covalent immobilization of soluble proteins on glass surfaces through an unnatural amino acid created by post-translationally modifying the cysteine residue in a CaaX recognition motif wit

SMALL MOLECULE COMPOSITIONS AND METHODS FOR INCREASING DRUG EFFICIENCY USING COMPOSITIONS THEREOF

In certain embodiments, provided herein are compositions and methods for increasing drug efficiency. The conjugates provided are in certain embodiments, for compositions and methods in treatment of variety of diseases and have the formula 1: D - L - S (1)

Toward Efficient Zn(II)-Based Artificial Nucleases

A series of cis-cis-triaminocyclohexane Zn(II) complex-anthraquinone intercalator conjugates, designed in such a way to allow their easy synthesis and modification, have been investigated as hydrolytic cleaving agents for plasmid DNA. The ligand structure

Structure-activity relationships in prazosin-related compounds. Effect of replacing a piperazine ring with an alkanediamine moiety on α1-adrenoreceptor blocking activity

Several prazosin-related compounds were synthesized in which the piperazine ring of prazosin (1) was replaced by an alkanediamine chain and were evaluated for their blocking activity on α1- and α2-adrenoreceptors in isolated rat vas