Building Blocks

Symmetrical functionalised aromatic

Bis[rhodium(±,±,±',±'-tetramethyl-1,3-benzenedipropionic Acid)] is a reagent that can be used in catalytic organic synthesis. Bis[rhodium(±,±,±',±'-tetramethyl-1,3-benzenedipropionic Acid)] is a stable compound that does not react with most organic solvents. It also has high solubility in many organic solvents. This reagent is toxicological and should be handled with care.

1-Azaspiro[3.5]nonane is a versatile building block with many uses in research and industrial chemistry. It can be used as a reagent for the synthesis of various organic compounds, or as an intermediate to synthesize more complex molecules. 1-Azaspiro[3.5]nonane is a high quality compound that is sold at a competitive price. The versatility of this compound makes it useful in many different reactions, and it can be used as a scaffold for the construction of more complex structures.

Versatile small molecule scaffold

Cis-2-Benzyltetrahydropyrrolo[3,4-C]Pyrrole-1,3(2H,3Ah)-Dione is a compound that is used as a chemical intermediate in the research and development of new medicines. It has been shown to be an effective building block for the synthesis of complex compounds with interesting biological activity.

1-(3-Azetidinyl)-pyrrolidine dihydrochloride is a high quality, versatile building block that can be used as a reagent in the synthesis of complex compounds and as an intermediate in the synthesis of fine chemicals. 1-(3-Azetidinyl)-pyrrolidine dihydrochloride is an excellent starting material for the synthesis of a wide range of compounds. It can also act as a speciality chemical or research chemical. 1-(3-Azetidinyl)-pyrrolidine dihydrochloride has CAS No. 1024589-68-1 and can be found on our website at www.chemistryworldstore.com

Versatile small molecule scaffold

Pyridine-2-sulfonamide is a synthetic drug that has been shown to inhibit the growth of cancer cells. It binds to the endothelin-A receptor, which is found in many tissues including the heart, brain, and skin. This binding inhibits the binding of epidermal growth factor to its receptor. Pyridine-2-sulfonamide also inhibits pancreatitis by inhibiting the production of hydrogen ions from hydrochloric acid and reducing inflammation. This drug has been shown to be effective against HIV infection.

Versatile small molecule scaffold

1-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopropan-1-amine is a high quality reagent that can be used as a useful intermediate in the synthesis of complex compounds. It has been shown to be a useful scaffold for the synthesis of various fine chemicals and speciality chemicals. 1-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopropan-1-amine is also versatile building block that can be used as a reaction component in many different chemical reactions.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

(1-Aminoethane-1,1-diyl)diphosphonic acid (HEDPA) is a synthetic phosphonate that is soluble in water and organic solvents. HEDPA has been used in gravimetric analysis because it is stable to boiling point and can be easily dried on the surface of a glass plate. It also has been used as a reagent for the synthesis of hydroxy methyl phosphonates and other phosphonate compounds. In crystal x-ray diffraction, HEDPA shows strong hydrogen bonding interactions with counterions such as PO43-, SO42-, or NH4+. The coordination chemistry of HEDPA involves metal ions such as Fe3+, Cu2+, Co2+, Ni2+, Cr3+, Mn2+, Zn2+, Cd2+ and Al3+. Functional theory predicts that the architecture of HEDPA's supramolecular units are either tetrahedral or octahedral. Inf

Versatile small molecule scaffold

Versatile small molecule scaffold

Phenyl sulfamate is a monosodium salt that has been shown to inhibit the growth of cancer cells in vitro. It has been used as an antimicrobial agent to treat chronic arthritis and atherosclerotic lesions. Phenyl sulfamate inhibits the activity of enzymes that are involved in the synthesis of proteins, such as collagenase, elastase, and proteases. The irreversible inhibition by phenyl sulfamate is due to its ability to react with sulfamoyl chloride (SOC). This reaction leads to the formation of a covalent bond between the enzyme and phenyl sulfamate, which cannot be reversed by any known chemical or enzymatic process.

Versatile small molecule scaffold