Aminobenzoic acids and derivatives
Chemscene 1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid | 25g | CS-W008223 | 98% | 113100-53-1 | MFCD01936005 | 194 11 | C6H5F3N2O2
Chemscene | 1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid | 25g | CS-W008223 | 98% | 113100-53-1 | MFCD01936005 | 194 11 | C6H5F3N2O2
Chemscene 2 6-Dimethylpiperazine | 25g | CS-W013629 | 98% | 108-49-6 | MFCD00005956 | 114 19 | C6H14N2
Chemscene | 2 6-Dimethylpiperazine | 25g | CS-W013629 | 98% | 108-49-6 | MFCD00005956 | 114 19 | C6H14N2
Chemscene (1R 3S)-1 2 2-Trimethylcyclopentane-1 3-dicarboxylic acid | 5g | CS-W015618 | 98% | 124-83-4 | MFCD00001375 | 200 23 | C10H16O4
Chemscene | (1R 3S)-1 2 2-Trimethylcyclopentane-1 3-dicarboxylic acid | 5g | CS-W015618 | 98% | 124-83-4 | MFCD00001375 | 200 23 | C10H16O4
Chemscene 2-Naphthoxyacetic acid | 500g | CS-W015512 | 98% | 120-23-0 | MFCD00004066 | 202 21 | C12H10O3
Chemscene | 2-Naphthoxyacetic acid | 500g | CS-W015512 | 98% | 120-23-0 | MFCD00004066 | 202 21 | C12H10O3
Chemscene Benzylideneacetone | 100g | CS-W013311 | 98% | 122-57-6 | MFCD00008779 | 146 19 | C10H10O
Chemscene | Benzylideneacetone | 100g | CS-W013311 | 98% | 122-57-6 | MFCD00008779 | 146 19 | C10H10O
Chemscene 7-Bromo-1H-indole-3-carbaldehyde | 1g | CS-W013076 | 98% | 115666-21-2 | MFCD06657151 | 224 057 | C9H6BrNO
Chemscene | 7-Bromo-1H-indole-3-carbaldehyde | 1g | CS-W013076 | 98% | 115666-21-2 | MFCD06657151 | 224 057 | C9H6BrNO
Chemscene 3-(4-(tert-Butyl)phenyl)propanoic acid | 5g | CS-W015310 | 98% | 1208-64-6 | MFCD00796482 | 206 28 | C13H18O2
Chemscene | 3-(4-(tert-Butyl)phenyl)propanoic acid | 5g | CS-W015310 | 98% | 1208-64-6 | MFCD00796482 | 206 28 | C13H18O2
Chemscene Methyl 5-(trifluoromethyl)picolinate | 10g | CS-W015384 | 98% | 124236-37-9 | MFCD08741523 | 205 13 | C8H6F3NO2
Chemscene | Methyl 5-(trifluoromethyl)picolinate | 10g | CS-W015384 | 98% | 124236-37-9 | MFCD08741523 | 205 13 | C8H6F3NO2
Chemscene (2 3 4-Trimethoxyphenyl)boronic acid | 100g | CS-W015030 | 98% | 118062-05-8 | MFCD01318183 | 212 01 | C9H13BO5
Chemscene | (2 3 4-Trimethoxyphenyl)boronic acid | 100g | CS-W015030 | 98% | 118062-05-8 | MFCD01318183 | 212 01 | C9H13BO5
Chemscene 3-Amino-2-chlorobenzoic acid | 1g | CS-W008322 | 98% | 108679-71-6 | MFCD00191726 | 171 58 | C7H6ClNO2
Chemscene | 3-Amino-2-chlorobenzoic acid | 1g | CS-W008322 | 98% | 108679-71-6 | MFCD00191726 | 171 58 | C7H6ClNO2
Chemscene 2-Fluoro-4-(trifluoromethyl)benzoic acid | 100g | CS-W015234 | 98% | 115029-24-8 | MFCD00010322 | 208 11 | C8H4F4O2
Chemscene | 2-Fluoro-4-(trifluoromethyl)benzoic acid | 100g | CS-W015234 | 98% | 115029-24-8 | MFCD00010322 | 208 11 | C8H4F4O2
Chemscene 1-(2-Bromo-4-fluorophenyl)ethanone | 1g | CS-W014824 | 98% | 1006-39-9 | MFCD00077464 | 217 037 | C8H6BrFO
Chemscene | 1-(2-Bromo-4-fluorophenyl)ethanone | 1g | CS-W014824 | 98% | 1006-39-9 | MFCD00077464 | 217 037 | C8H6BrFO
Medchemexpress LLC Almitrine mesylate | 29608-49-9 | MFCD01679060 | 99.8% | 669.76 g·mol-1 | C28H37F2N7O6S2 | 100 MG
Almitrine mesylate is a research-grade peripheral chemoreceptor agonist that selectively inhibits Ca2+-dependent K+ channels, used in studies of ventilatory control and pulmonary vascular responses. Supplied as a high-purity salt with solubility and storage guidance for laboratory use.
- High purity (99.8%).
- Molecular weight 669.76 g·mol-1; formula C28H37F2N7O6S2.
- Soluble in DMSO (≈100 mg/mL); in vivo vehicle protocols provided.
- Suitable for in vitro and in vivo pharmacological studies.
- Solid storage at 4°C; in solution store at -80°C up to 6 months.
- Available in small research pack sizes and larger quantities by quote.
Medchemexpress LLC D-mannopyranose, 1,2,3,4,6-penta-O-acetyl | 25941-03-1 | MFCD05864874 | 98.0% | 390.34 | C16H22O11 | 25 G
1,2,3,4,6-Penta-O-acetyl-D-mannopyranose is an acetyl-protected derivative of D-mannopyranose used as a synthetic intermediate in carbohydrate chemistry. It is supplied as a solid with molecular formula C16H22O11 and molecular weight 390.34 g/mol. Typical applications include glycoside synthesis and preparative carbohydrate modifications.
- Acetyl-protected hydroxyl groups facilitate selective glycosylation reactions.
- Suitable for synthesis of tetra-O-acetyl-O-prop-1-yl-α-D-mannopyranoside and related derivatives.
- Available in small pack sizes appropriate for laboratory synthesis.
- Characterized by standard chemical identifiers and documented analytical data.
- Supplied with batch-specific certificate of analysis for quality verification.