Aminobenzoic acids and derivatives
STA Pharmaceutical 2-(Fmoc-amino)-4-chlorobenzoic acid | 10 g | CAS 332121-92-3 | MDL MFCD02682157
2-(Fmoc-amino)-4-chlorobenzoic acid is a Amino Acid reagent (Subcategory: Unusual AA) sold by WuXi TIDES. Offered in 10 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 332121-92-3
- MDL: MFCD02682157
- InChIKey: BIPQSYSWHUYDEA-UHFFFAOYSA-N
- Molecular Weight: 393.823
- Molecular Formula: C22H16ClNO4
- Purity: ≥95%
- Container Type: 60 mL HDPE
- Pack Size: 10 g
- Net Weight: 10 g
- Gross Weight: 25 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-chlorobenzoic acid
- SMILES: ClC1=CC(NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)=C(C=C1)C(O)=O
Cayman Chemical 3-HydroxypIcolInIc AcId 25g
A matrix substance for MALDI-MS; has been used in the analysis of oligonucleotides and proteins; has been used as a complexation agent for metal complexes; is an intermediate in the biosynthesis of virginiamycin S1
Aobchem 2-(Cyclobutylmethoxy)benzoic acid | 95% | CAS 1047680-59-0 | C12H14O3 | 500mg
2-(Cyclobutylmethoxy)benzoic acid | 95% | CAS 1047680-59-0 | C12H14O3 | 500mg
Aobchem Benzoic acid 3-(5-chloro-2-pyridinyl)- | 97% | CAS 1286126-96-2 | C12H8ClNO2 | 1g
Benzoic acid 3-(5-chloro-2-pyridinyl)- | 97% | CAS 1286126-96-2 | C12H8ClNO2 | 1g
Aobchem Benzoic acid 3-(5-chloro-2-pyridinyl)- | 97% | CAS 1286126-96-2 | C12H8ClNO2 | 500mg
Benzoic acid 3-(5-chloro-2-pyridinyl)- | 97% | CAS 1286126-96-2 | C12H8ClNO2 | 500mg
Aobchem Benzoic acid 3-(5-chloro-2-pyridinyl)- | 97% | CAS 1286126-96-2 | C12H8ClNO2 | 250mg
Benzoic acid 3-(5-chloro-2-pyridinyl)- | 97% | CAS 1286126-96-2 | C12H8ClNO2 | 250mg
Chemscene Ethyl 6-bromo-4-hydroxyquinoline-3-carboxylate | 100g | CS-M0117 | 95% | 122794-99-4 | MFCD00173362 | 296 12 | C12H10BrNO3
Chemscene | Ethyl 6-bromo-4-hydroxyquinoline-3-carboxylate | 100g | CS-M0117 | 95% | 122794-99-4 | MFCD00173362 | 296 12 | C12H10BrNO3
Aobchem 1-(3-Chloro-5-(dimethylamino)phenyl)propan-1-one | 95% | C11H14ClNO | 1g
1-(3-Chloro-5-(dimethylamino)phenyl)propan-1-one | 95% | C11H14ClNO | 1g
Chemscene 1 5-Dihydroxypentane | 1kg | CS-W020635 | 98% | 111-29-5 | MFCD00002978 | 104 15 | C5H12O2
Chemscene | 1 5-Dihydroxypentane | 1kg | CS-W020635 | 98% | 111-29-5 | MFCD00002978 | 104 15 | C5H12O2
Chemscene 2-Bromopyridine-4-methanol | 10g | CS-W000831 | 98% | 118289-16-0 | MFCD04039313 | 188 024 | C6H6BrNO
Chemscene | 2-Bromopyridine-4-methanol | 10g | CS-W000831 | 98% | 118289-16-0 | MFCD04039313 | 188 024 | C6H6BrNO
Aobchem 4-((2-Methylbenzyl)oxy)benzoic acid | 97% | CAS 149289-01-0 | C15H14O3 | 1g
4-((2-Methylbenzyl)oxy)benzoic acid | 97% | CAS 149289-01-0 | C15H14O3 | 1g
Medchemexpress LLC Alpha-Ionone | 127-41-3 | MFCD00001565 | 192.30 | 1 ML
Alpha-Ionone (α-Ionone) is a chemical compound with the molecular formula C13H20O and a molecular weight of 192.30. It functions as an activator of the olfactory receptor OR10A6 and is known to induce apoptosis by stimulating the LATS-YAP-TAZ signaling axis within the Hippo pathway. This compound demonstrates inhibitory effects on tumor formation both in vitro and in vivo. It targets various pathways including Hippo (MST), YAP, Olfactory Receptor, and Apoptosis.
- Activates olfactory receptor OR10A6
- Induces apoptosis by activating LATS-YAP-TAZ signaling
- Inhibits tumor formation in vitro and in vivo
- Increases cAMP in A431 cells with an EC50 of 152.4 μM
- Inhibits proliferation and migration of A431 and HaCaT cells
- Modulates key proteins involved in apoptosis, including caspase-3, BAX, and BCL-2
- Suppresses growth of A431 cell xenograft in animal models
Aobchem 3-Cyclobutyl-5-methylbenzoic acid | 95% | CAS 2921879-89-0 | C12H14O2 | 250mg
3-Cyclobutyl-5-methylbenzoic acid | 95% | CAS 2921879-89-0 | C12H14O2 | 250mg
Medchemexpress LLC Diphenylacetic acid | 117-34-0 | MFCD00004251 | 99.8% | 212.25 g/mol | C14H12O2 | 100g
Diphenylacetic acid (Diphenylmethane- -carboxylic Acid) is a biochemical reagent that can be used as a biological material or organic compound for life science related research Diphenylacetic acid can be used as a reagent in the kinetic resolution of racemic 2-hydroxy-y-butyrolactones by asymmetric esterification in the presence of pivalic anhydride and chiral acyl-transfer catalyst Diphenylacetic acid can act as a catalyst to synthesize 2-allyl-3-oxazolin-5-one derivatives via Rh-catalyzed coupling reaction of azlactones and alkynes followed by aza-Cope rearrangement[1][2][3][4]
Aobchem 2-Bromo-7-methylbenzo[b]thiophene | 95% | CAS 1824077-88-4 | C9H7BrS | 1g
2-Bromo-7-methylbenzo[b]thiophene | 95% | CAS 1824077-88-4 | C9H7BrS | 1g