Thiazoles
Methyl 2-Bromothiazole-5-carboxylate 95.0+%, TCI America™
CAS: 54045-74-8 Molecular Formula: C5H4BrNO2S Molecular Weight (g/mol): 222.056 MDL Number: MFCD03788565 InChI Key: HNLVIKMXFBRZDF-UHFFFAOYSA-N Synonym: methyl 2-bromothiazole-5-carboxylate,methyl 2-bromo-5-thiazole carboxylate,methyl2-bromothiazole-5-carboxylate,5-thiazolecarboxylic acid, 2-bromo-, methyl ester,2-bromo-thiazole-5-carboxylic acid methyl ester,2-bromothiazole-5-carboxylic acid methyl ester,2-bromo-1,3-thiazole-5-carboxylic acid methyl ester,pubchem17197,acmc-1apjm,ksc494s7p PubChem CID: 2773502 IUPAC Name: methyl 2-bromo-1,3-thiazole-5-carboxylate SMILES: COC(=O)C1=CN=C(S1)Br
Methyl 2-Aminothiazole-4-carboxylate 98.0+%, TCI America™
CAS: 118452-04-3 Molecular Formula: C5H6N2O2S Molecular Weight (g/mol): 158.175 MDL Number: MFCD00622441 InChI Key: WYVZZWKIKAKUKV-UHFFFAOYSA-N Synonym: 2-Aminothiazole-4-carboxylic Acid Methyl Ester PubChem CID: 840099 IUPAC Name: methyl 2-amino-1,3-thiazole-4-carboxylate SMILES: COC(=O)C1=CSC(=N1)N
Ethyl 4-Methylthiazole-5-carboxylate 97.0+%, TCI America™
CAS: 20582-55-2 Molecular Formula: C7H9NO2S Molecular Weight (g/mol): 171.214 MDL Number: MFCD00626873 InChI Key: WISQBJLUORKXNY-UHFFFAOYSA-N Synonym: ethyl 4-methylthiazole-5-carboxylate,5-thiazolecarboxylic acid, 4-methyl-, ethyl ester,4-methyl-5-thiazolecarboxylic acid ethyl ester,5-thiazolecarboxylic acid, 4-methyl-ethylester,4-methyl-thiazole-5-carboxylic acid ethyl ester,4-methylthiazole-5-carboxylic acid ethyl ester,ethyl4-methyl-5-thiazoleactate,ethylmethylthiazolecarboxylate,4-methyl-5-ethoxycarbonyl thiazole,4-methylthiazol-5-carbonsaureathylester PubChem CID: 298610 IUPAC Name: ethyl 4-methyl-1,3-thiazole-5-carboxylate SMILES: CCOC(=O)C1=C(N=CS1)C
Ethyl 2-Bromothiazole-4-carboxylate 95.0+%, TCI America™
CAS: 100367-77-9 Molecular Formula: C6H6BrNO2S Molecular Weight (g/mol): 236.083 MDL Number: MFCD03788564 InChI Key: CNHISCQPKKGDPO-UHFFFAOYSA-N PubChem CID: 353965 IUPAC Name: ethyl 2-bromo-1,3-thiazole-4-carboxylate SMILES: CCOC(=O)C1=CSC(=N1)Br
Ethyl 2-Aminothiazole-4-carboxylate 98.0+%, TCI America™
CAS: 5398-36-7 Molecular Formula: C6H8N2O2S Molecular Weight (g/mol): 172.202 MDL Number: MFCD00619079 InChI Key: XHFUVBWCMLLKOZ-UHFFFAOYSA-N Synonym: ethyl 2-aminothiazole-4-carboxylate,2-amino-thiazole-4-carboxylic acid ethyl ester,ethyl 2-amino-4-thiazolecarboxylate,4-thiazolecarboxylic acid, 2-amino-, ethyl ester,ethyl 2-amino-4-thiazoleformate,2-amino-4-ethoxycarbonylthiazole,2-aminothiazole-4-ethyl formate,2-aminothiazole-4-carboxylic acid ethyl ester,ethyl-2-aminothiazole-4-carboxylate,ethyl-2-aminothiazole-4-carboxylic acid PubChem CID: 73216 IUPAC Name: ethyl 2-amino-1,3-thiazole-4-carboxylate SMILES: CCOC(=O)C1=CSC(=N1)N
Methyl 2-Bromothiazole-4-carboxylate 98.0+%, TCI America™
CAS: 170235-26-4 Molecular Formula: C5H4BrNO2S Molecular Weight (g/mol): 222.056 MDL Number: MFCD06659908 InChI Key: YOWKNNKTQWCYNC-UHFFFAOYSA-N PubChem CID: 2763213 IUPAC Name: methyl 2-bromo-1,3-thiazole-4-carboxylate SMILES: COC(=O)C1=CSC(=N1)Br
Methyl 2-Aminothiazole-5-carboxylate 98.0+%, TCI America™
CAS: 6633-61-0 Molecular Formula: C5H6N2O2S Molecular Weight (g/mol): 158.175 MDL Number: MFCD03788562 InChI Key: UJNNCGWBDJHCEM-UHFFFAOYSA-N Synonym: 2-Aminothiazole-5-carboxylic Acid Methyl Ester PubChem CID: 238005 IUPAC Name: methyl 2-amino-1,3-thiazole-5-carboxylate SMILES: COC(=O)C1=CN=C(S1)N
Matrix Scientific METHYL 2-AMINOTHIAZOLE-4-CA-5G
Methyl 2-aminothiazole-4-carboxylate, 95%-5g,C5H6N2O2S, MFCD00622441, mw 158.18,
Apexbio Technology LLC MTT(Synonyms: Thiazolyl Blue Tetrazolium Bromide, Methylthiazolyldiphenyl-tetrazolium bromide), 500mg, CAS: 298-93-1.
MTT (CAS 298-93-1) chemically known as 3-(4 5-Dimethylthiazol-2-yl)-2 5-diphenyl-2H-tetrazolium bromide is a tetrazolium salt commonly employed in biomedical research to assess cellular proliferation and metabolic activity in vitro Upon uptake by viable cells MTT undergoes reduction primarily mediated by NADH-dependent oxidoreductases in mitochondria and partly by extra-mitochondrial enzymes forming insoluble formazan precipitates The resulting formazan accumulation correlates with metabolic activity and cell viability Due to its membrane-permeable cationic nature MTT efficiently penetrates intact cell membranes without requiring intermediates distinguishing it from second-generation negatively charged tetrazolium derivatives
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Sigma Aldrich 3-[Bis(2-hydroxyethyl)amino]propyl-triethoxysilane solution
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Sigma Aldrich 5-Amino-3-methyl-isothiazole hydrochloride
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Sigma Aldrich Sodium 4-hydroxybenzenesulfonate dihydrate
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Sigma Aldrich 2-Nitrophenylacetic acid
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Sigma Aldrich 4-Bromo-2-nitrophenol
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Sigma Aldrich 2,4-Dichlorophenylacetic acid
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