Cetrimonium bromide

(11-Mercaptoundecyl)- N,N,N -trimethylammonium bromide (MABr) is an organothiol which forms a self-assembled monolayer (SAM) that facilitates the immobilization of a variety of nanoparticles. Application MABr can be used to functionalize gold

(11bS)-(+)-4,4-Dibutyl-4,5-dihydro-2,6-bis(3,4,5-trifluorophenyl)-3H-dinaphth[2,1-c:1',2'-e]azepinium bromide

(1 S - cis )-3-Bromo-3,5-cyclohexadiene-1,2-diol is a chiral cis -dienediol employed as a key building block for the preparation of varieties of natural products. It can undergo few chemical reactions like cycloadditions, sigmatropic

(Bromomethyl)cyclohexane

(Bromomethyl)cyclohexane

(Bromomethyl)cyclohexane

(Bromomethylene)dimethyliminium bromide participates in one-carbon homologation of aldehydes to carboxylic acid derivatives. Application (Bromomethylene)dimethyliminium bromide (bromodi- methylformiminium bromide) may be employed for the synthesis

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

(E)-2-Bromo-2-butene

Biochem/physiol Actions Selective acetylcholinesterase inhibitor. Features and Benefits This compound is featured on the Acetylcholine Synthesis and Metabolism page of the Handbook of Receptor Classification and Signal Transduction.

Biochem/physiol Actions Selective acetylcholinesterase inhibitor. Features and Benefits This compound is featured on the Acetylcholine Synthesis and Metabolism page of the Handbook of Receptor Classification and Signal Transduction.

Biochem/physiol Actions Selective acetylcholinesterase inhibitor. Features and Benefits This compound is featured on the Acetylcholine Synthesis and Metabolism page of the Handbook of Receptor Classification and Signal Transduction.