Building Blocks
Subcategories of "Building Blocks"
- Boronic Acids & Boronic Acid Derivatives(5,780 products)
- Chiral Building Blocks(1,241 products)
- Hydrocarbon Building Blocks(6,100 products)
- Organic Building Blocks(61,029 products)
Found 205306 products of "Building Blocks"
N7-Benzylpyrimido[4,5-d]pyrimidine-2,4,7-triamine
CAS:Versatile small molecule scaffoldFormula:C13H13N7Purity:Min. 95%Molecular weight:267.29 g/mol3-{5,6-Dimethyl-4-oxo-1H,4H-thieno[2,3-d]pyrimidin-2-yl}propanoic acid
CAS:Controlled Product3-{5,6-Dimethyl-4-oxo-1H,4H-thieno[2,3-d]pyrimidin-2-yl}propanoic acid is an antibody that blocks the activity of ion channels and has a high purity. It is used in cell biology research and as a pharmacological research tool. 3DMPPA is a receptor antagonist and can be used to inhibit or activate the function of peptides or ligands. 3DMPPA binds to receptors on cells, blocking the binding of other compounds and preventing them from activating the receptor. This compound can also be used as an inhibitor or activator of ion channels. 3DMPPA has been shown to have antiinflammatory effects on animal models, which may be due to its inhibition of prostaglandin synthesis by inhibiting cyclooxygenase 1 (COX1) and cyclooxygenase 2 (COX2).Formula:C11H12N2O3SPurity:Min. 95%Molecular weight:252.29 g/mol3-{3-Oxo-8-thia-4,6-diazatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),4-trien-5-yl}propanoic acid
CAS:Versatile small molecule scaffoldFormula:C13H14N2O3SPurity:Min. 95%Molecular weight:278.33 g/mol2-bromo-3-methylbenzaldehyde
CAS:2-Bromo-3-methylbenzaldehyde is an enantiomerically pure stereogenic aldehyde that can be used in the synthesis of quinoline derivatives. This compound has been shown to interact with biomolecules and induce chiral effects. It is also a photochromic molecule that reacts with ultraviolet light to change color, which can be used in the design of cyclic and dihedral molecules. The selective reaction of 2-bromo-3-methylbenzaldehyde with alkyl halides leads to diastereoselective or stereoselective reactions. This compound has been shown to have high yields for these reactions.
Formula:C8H7BrOPurity:Min. 95%Molecular weight:199 g/mol1-Benzofuran-2-yl(phenyl)methanamine hydrochloride
CAS:Versatile small molecule scaffoldFormula:C15H14ClNOPurity:Min. 95%Molecular weight:259.73 g/mol6-Bromo-3,4-dihydro-2H-1-benzothiopyran
CAS:Versatile small molecule scaffoldFormula:C9H9BrSPurity:Min. 95%Molecular weight:229.14 g/molMethyl-d3 1-Methyl-d3-1H-indazole-3-carboxylate
CAS:Controlled ProductMethyl-d3 1-Methyl-d3-1H-indazole-3-carboxylate (MDI) is a reagent used in the synthesis of organic compounds. It is formed by the reaction of lithium aluminum hydride and methyl acetate, which produces a lithiated carboxylic acid. This compound can be reacted with amines to form amides or with thionyl chloride to form sulfonyl chlorides. The reactions are reversible, so it can be regenerated when needed.
Formula:C10H4D6N2O2Purity:Min. 95%Molecular weight:196.24 g/molMethyl 2-methyl-2H-indazole-3-carboxylate
CAS:Controlled ProductVersatile small molecule scaffoldFormula:C10H10N2O2Purity:Min. 95%Molecular weight:190.2 g/mol4-{5H,6H,7H,8H,9H-[1,2,4]Triazolo[4,3-a]azepin-3-yl}aniline
CAS:Versatile small molecule scaffoldFormula:C13H16N4Purity:Min. 95%Molecular weight:228.29 g/mol(2-Phenoxy-phenyl)-hydrazine HCl
CAS:Versatile small molecule scaffoldFormula:C12H12N2O·HClPurity:Min. 95%Molecular weight:236.7 g/mol4H,5H-Imidazo[1,2-a]quinazolin-5-one
CAS:Versatile small molecule scaffoldFormula:C10H7N3OPurity:Min. 95%Molecular weight:185.18 g/mol3H,4H,5H,6H,7H,8H-Pyrido[4,3-d]pyrimidin-4-one dihydrochloride
CAS:Versatile small molecule scaffoldFormula:C7H11Cl2N3OPurity:Min. 95%Molecular weight:224.08 g/mol4-(2,2,3,3-Tetrafluoropropoxy)aniline hydrochloride
CAS:Versatile small molecule scaffoldFormula:C9H10ClF4NOPurity:Min. 95%Molecular weight:259.63 g/mol1-(4-bromophenyl)cyclopropan-1-ol
CAS:1-(4-bromophenyl)cyclopropan-1-ol is an unsaturated, halide reagent that is used to cyclopropanate olefins. It reacts with allylic alcohols and allylic amines to form allylic ethers and amides respectively. 1-(4-Bromophenyl)cyclopropan-1-ol can be used as a diazomethane source for the synthesis of nitrogen containing compounds. This reagent also reacts with allyl alcohols to form vinyl bromides or vinyl iodides. The reaction of 1-(4-bromophenyl)cyclopropan-1-ol with olefins yields sterically hindered alcohols and ethers.Formula:C9H9BrOPurity:Min. 95%Molecular weight:213.07 g/molN,N-Dibenzyl-2-chloropropanamide
CAS:Versatile small molecule scaffoldFormula:C17H18ClNOPurity:Min. 95%Molecular weight:287.8 g/mol2-[4-(Benzyloxy)-1H-indol-3-yl]ethan-1-amine
CAS:Controlled ProductVersatile small molecule scaffoldFormula:C17H18N2OPurity:Min. 95%Molecular weight:266.3 g/mol2,2-Dimethyl-1-phenylcyclopropan-1-amine
CAS:Versatile small molecule scaffoldFormula:C11H15NPurity:Min. 95%Molecular weight:161.24 g/mol2-(3-Phenoxyphenyl)acetaldehyde
CAS:Versatile small molecule scaffoldFormula:C14H12O2Purity:Min. 95%Molecular weight:212.2 g/mol2-(3,4-Difluorophenyl)acetaldehyde
CAS:Versatile small molecule scaffoldFormula:C8H6F2OPurity:Min. 95%Molecular weight:156.13 g/mol2-(4-tert-Butylphenyl)acetaldehyde
CAS:Versatile small molecule scaffoldFormula:C12H16OPurity:Min. 95%Molecular weight:176.25 g/mol
