Furfuryl mercaptan,98-02-2,Phenylmethylsulfonyl fluoride,329-98-6

Bortezomib 179324-69-7 MFCD05260688
Bortezomib is used to treat people with multiple myeloma (a type of cancer of the bone marrow) who have already been treated with at least one other medication. Bortezomib is also used to treat people with mantle cell lymphoma (a fast-growing cancer that begins in the cells of the immune system) who have already been treated with at least one other medication. Bortezomib is in a class of medications called antineoplastic agents. It works by killing cancer cells.
Indole-3-acetic acid 87-51-4 MFCD00005636

Actinomycin D 50-76-0 MFCD00070921

2,3-Dimethylpyrazine 5910-89-4 MFCD00197755

Coelenteramine 55779-48-1 MFCD00467176

Coelenteramine  is the luciferin, the light-emitting molecule, found in many aquatic organisms across seven phyla.It is the substrate in many luciferases and photoproteins including Renilla reniformis luciferase (Rluc), Gaussia luciferase (Gluc), aequorin, and obelin.

Coelenterazine was simultaneously isolated and characterized by two groups studying the luminescent organisms Sea pansy Renilla reniformis and the coelenterate Aequorea victoria, respectively.Both groups unknowingly discovered that the same compound was used in both luminescent systems, however the name of the molecule was given after the coelenterate. Likewise, the two main metabolites - coelenteramide and coelenteramine - were named after their respective functional groups.


BES 10191-18-1 MFCD00007533

EPPS 16052-06-5 MFCD00006160

Furfuryl mercaptan 98-02-2 MFCD00003254

Phenylmethylsulfonyl fluoride 329-98-6 MFCD00007421

2-Methyltetrahydrofuran-3-one 3188-00-9 MFCD00010423

3,5-DIFLUOROTOLUENE,117358-51-7,3-Bromofluorobenzene,1073-06-9

3,5-DIFLUOROTOLUENE 117358-51-7 MFCD00797323

3-Cyano-4-fluorobenzotrifluoride 4088-84-0 MFCD00061280

2,4,5-Trifluorophenylacetic acid 209995-38-0 MFCD00082479

2,6-DIFLUOROPHENYLACETONITRILE 654-01-3 MFCD00009973

3-BROMO-4-HYDROXYBENZONITRILE 2315-86-8 MFCD00143096

2,4,6-Trichlorobenzoic acid 50-43-1 MFCD00060699

3-Bromofluorobenzene 1073-06-9 MFCD00000326

2,3-Difluorophenol 6418-38-8 MFCD00010262

3-FLUORO-4-(TRIFLUOROMETHYL)BENZOIC ACID 115754-21-7 MFCD00236279

3,5-Dicyanofluorobenzene 453565-55-4 MFCD05663831

6-Bromoquinoline,5332-25-2,4-Fluoroindole,387-43-9

3,4-DIAMINOBENZOTRIFLUORIDE 368-71-8 MFCD00042456

2-Cyclopentenone 930-30-3 MFCD00001401

6-Bromoquinoline 5332-25-2 MFCD00024023

4-Fluoro-2-methylbenzonitrile 147754-12-9 MFCD03095106

1-Fluoro-4-iodobenzene 352-34-1 MFCD00001052

Iodobenzene is commercially available, but it may be prepared in the laboratory from aniline via the Sandmeyer reaction. In the first step, the amine functional group is diazotized with hydrochloric acid and sodium nitrite. Potassium iodide is added to the resultant diazonium chloride, causing nitrogen gas to evolve. Any excess nitrite is hydrolyzed with a strong base; the mixture is acidified and the desired product is separated by steam distillation.


4-(Trifluoromethoxy)anisole 710-18-9 MFCD00216942

2,3,4-Trifluorobenzoic acid 61079-72-9 MFCD00061232

3-FLUORO-5-(TRIFLUOROMETHYL)BENZOYL CHLORIDE 171243-30-4 MFCD00061157

4-Fluoroindole 387-43-9 MFCD00055992

1-Chloro-3,4-difluorobenzene 696-02-6 MFCD00042572