Building Blocks
This section contains fundamental products for the synthesis of organic and biological compounds. Building blocks are the essential starting materials used to construct complex molecules through various chemical reactions. They play a critical role in drug discovery, material science, and chemical research. At CymitQuimica, we offer a diverse range of high-quality building blocks to support your innovative research and industrial projects, ensuring you have the essential components for successful synthesis.
Subcategories of "Building Blocks"
- Boronic Acids & Boronic Acid Derivatives(5,778 products)
- Chiral Building Blocks(1,243 products)
- Hydrocarbon Building Blocks(6,098 products)
- Organic Building Blocks(61,036 products)
Found 205240 products of "Building Blocks"
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2-[(Pyridin-3-ylmethyl)amino]benzoic acid
CAS:Versatile small molecule scaffoldFormula:C13H12N2O2Purity:Min. 95%Molecular weight:228.25 g/mol3-(3,4-Dichlorophenyl)-2-sulfanyl-3,4-dihydroquinazolin-4-one
CAS:Versatile small molecule scaffoldFormula:C14H8Cl2N2OSPurity:Min. 95%Molecular weight:323.2 g/mol3-(2-Hydroxyethyl)piperidin-2-one
CAS:Versatile small molecule scaffold
Formula:C7H13NO2Purity:Min. 95%Molecular weight:143.18 g/mol(S)-2-Methoxypropan-1-amine hydrochloride
CAS:Versatile small molecule scaffold
Formula:C4H11NO·HClPurity:Min. 95%Molecular weight:125.59 g/mol3-(Prop-2-yn-1-yl)piperidin-2-one
CAS:Versatile small molecule scaffoldFormula:C8H11NOPurity:Min. 95%Molecular weight:137.18 g/mol3-(Propan-2-yl)piperidin-2-one
CAS:3-(Propan-2-yl)piperidin-2-one is an antimicrobial agent that has antibacterial activity. It inhibits the growth of bacteria and fungi by binding to the 50S ribosomal subunit. 3-(Propan-2-yl)piperidin-2-one has a greater inhibitory effect on bacteria than it does on fungi. This compound also binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 3-(Propan-2-yl)piperidin-2-one is synthesized from 2,6-dichloropyrimidine and ethyl propanoate in vitro, which are both available commercially. The nmr spectra of this compound were analysed and found to be consistent with those of its synthetic counterpart. 3-(Propan-2-yl)piperidin-2-one was found toFormula:C8H15NOPurity:Min. 95%Molecular weight:141.21 g/mol5-Bromo-3-chloro-1,2-benzothiazole
CAS:Versatile small molecule scaffoldFormula:C7H3BrClNSPurity:Min. 95%Molecular weight:248.53 g/molMethyl 4-formyloxane-4-carboxylate
CAS:Versatile small molecule scaffold
Formula:C8H12O4Purity:Min. 95%Molecular weight:172.18 g/mol2-Fluoro-6-(2,2,2-trifluoroethoxy)-benzaldehyde
CAS:Versatile small molecule scaffold
Formula:C9H6F4O2Purity:Min. 95%Molecular weight:222.14 g/moltert-Butyl 2-formylbenoate
CAS:Versatile small molecule scaffoldFormula:C12H14O3Purity:Min. 95%Molecular weight:206.24 g/mol4-chloro-5-nitro-1h-indazole
CAS:Versatile small molecule scaffoldFormula:C7H4ClN3O2Purity:Min. 95%Molecular weight:197.58 g/molN-Methoxy-N-methyloxolane-2-carboxamide
CAS:Versatile small molecule scaffoldFormula:C7H13NO3Purity:Min. 95%Molecular weight:159.18 g/mol2-Amino-4H-thieno[2,3-c]chromene-1-carbonitrile
CAS:Versatile small molecule scaffoldFormula:C12H8N2OSPurity:Min. 95%Molecular weight:228.27 g/mol1-{5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}ethan-1-one
CAS:Versatile small molecule scaffoldFormula:C9H10N4OPurity:Min. 95%Molecular weight:190.2 g/mol1-(2,2,2-Trifluoroethyl)piperazin-2-one
CAS:Versatile small molecule scaffoldFormula:C6H9F3N2OPurity:Min. 95%Molecular weight:182.14 g/mol1-Cyclopropylpiperazin-2-one
CAS:Versatile small molecule scaffoldFormula:C7H12N2OPurity:Min. 95%Molecular weight:140.18 g/mol4,7-Diazaspiro[2.5]octan-8-one
CAS:Versatile small molecule scaffoldFormula:C6H10N2OPurity:Min. 95%Molecular weight:126.16 g/mol5,8-Diaza-spiro[3.5]nonan-9-one
CAS:Versatile small molecule scaffold
Formula:C7H12N2OPurity:Min. 95%Molecular weight:140.18 g/mol5-Methyl-2-piperazinone HCl
CAS:5-Methyl-2-piperazinone HCl is an efficient synthetic intermediate that can be used for the synthesis of amines, cyclization, and reductive coupling. It is prepared by the reaction of methyl piperazine with aqueous hydrochloric acid to give 5-methyl-2-piperazinone. The chemical structure of this compound consists of a benzene ring substituted with two methyl groups at the nitrogen atom. This chemical intermediate can be used in reductive coupling with amines to produce secondary amines or in reductive coupling with alcohols to produce primary amines.
5-Methyl-2-piperazinone HCl also reacts efficiently with carbonyl compounds in an amination reaction to produce tertiary amines.Formula:C5H11ClN2OPurity:Min. 95%Molecular weight:150.61 g/mol5-(Propan-2-yl)piperazin-2-one
CAS:Versatile small molecule scaffoldFormula:C7H14N2OPurity:Min. 95%Molecular weight:142.2 g/mol
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![2-Amino-4H-thieno[2,3-c]chromene-1-carbonitrile](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FHLB96253.webp&w=3840&q=75)
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![5,8-Diaza-spiro[3.5]nonan-9-one](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FHLB97303.webp&w=3840&q=75)
