Nitrophenols
2,6-Dinitro-4-(trifluoromethyl)phenol 97.0+%, TCI America™
CAS: 393-77-1 Molecular Formula: C7H3F3N2O5 Molecular Weight (g/mol): 252.105 MDL Number: MFCD00194260 InChI Key: FXZGYEWQIGIFMC-UHFFFAOYSA-N Synonym: 4-Hydroxy-3,5-dinitrobenzotrifluoride, alpha,alpha,alpha-Trifluoro-2,6-dinitro-p-cresol PubChem CID: 164591 IUPAC Name: 2,6-dinitro-4-(trifluoromethyl)phenol SMILES: C1=C(C=C(C(=C1[N+](=O)[O-])O)[N+](=O)[O-])C(F)(F)F
Cell Signaling Technology Dinitrophenol (D1D6) Rabbit mAb 20 ul
Dinitrophenol (D1D6) Rabbit mAb 20 ul
Sigma Organic Chemistry 2 4-Dinitrophenol | 1KG | 51-28-5 | MFCD00007115
2,4-Dinitrophenol, 1KG
About This Item:
Storage: room temp
Chem-Impex International, Inc. 3,5-Dinitrosalicylic acid | 609-99-4 | MFCD00007104 | 100G
3,5-Dinitrosalicylic acid, 609-99-4, MFCD00007104, 100G
Selleck Chemical LLC FHD-609-E1859-25MG
FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit
Selleck Chemical LLC FHD-609-E1859-100MG
FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit
Selleck Chemical LLC STO-609
STO-609 is a specific inhibitor of the Ca2 /Calmodulin-dependent protein kinase kinase(CaM-KK) that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ng/ml respectively and also inhibits their autophosphorylation activities STO-609 inhibits AMPKK activity and inhibits autophagy
Selleck Chemical LLC STO-609
STO-609 is a specific inhibitor of the Ca2 /Calmodulin-dependent protein kinase kinase(CaM-KK) that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ng/ml respectively and also inhibits their autophosphorylation activities STO-609 inhibits AMPKK activity and inhibits autophagy
Selleck Chemical LLC FHD-609-E1859-1G
FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit
TARGETMOL CHEMICALS INC A 21960 5MG
Also available in 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. A 21960 (Ethyl 2-chloroacetoacetate) inhibits synapse formation between resolvase and two directly repeated res sites blocks site-specific recombination reactions and can be used to study bacterial infections. purity: 99%
eMolecules 2,6-Dinitro-p-cresol, wetted with ca 20% of water | 609-93-8 | MFCD00007121 | 1g
Combi-Blocks | 2,6-Dinitro-p-cresol, wetted with ca 20% of water | 1g | 342866343 | QG-0457 | 95.000 | 609-93-8 | MFCD00007121 | 198.134 | C7H6N2O5
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eMolecules 2-Nitrophenol sodium salt | 824-39-5 | MFCD00065178 | 5g
Combi-Blocks | 2-Nitrophenol sodium salt | 5g | 205396993 | QA-1640 | 98.000 | 824-39-5 | MFCD00065178 | 161.092 | C6H4NNaO3
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eMolecules 3-Hydroxybenzoic acid sodium salt | 7720-19-6 | MFCD00058986 | 1g
Combi-Blocks | 3-Hydroxybenzoic acid sodium salt | 1g | 401042805 | QE-7458 | 96.000 | 7720-19-6 | MFCD00058986 | 160.104 | C7H5NaO3
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