Bromobenzenes

Organic compounds considered aryl halides that consist of a phenyl group with a bromine atom substitution in the following structure: C₆H₅Br.

1,216 – 1,230 of 1,632 results

1,216

Chemscene ChemScene | 2,6-Dibromo-4-fluorobenzonitrile | 5G | CS-0161492 | 0.98 | 404928-18-3| MFCD24387472 | 278.91

ChemScene | 2,6-Dibromo-4-fluorobenzonitrile | 5G | CS-0161492 | 0.98 | 404928-18-3| MFCD24387472 | 278.91

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1,217

eMolecules 2-BROMO-5-FLUORO-4-NITROBENZOIC ACID | 1805189-72-3 | MFCD28739985 | 1g

AstaTech | 2-BROMO-5-FLUORO-4-NITROBENZOIC ACID | 1g | 624127234 | AC4831 | 95.000 | 1805189-72-3 | MFCD28739985 | 264.006 | C7H3BrFNO4

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1,218

eMolecules 2-Nitro-4-(trifluoromethoxy)phenol | 129644-56-0 | MFCD03094188 | 1g

Apollo Scientific | 2-Nitro-4-(trifluoromethoxy)phenol | 1g | 562451922 | PC2782 | | 129644-56-0 | MFCD03094188 | 223.107 | C7H4F3NO4

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1,219

Medchemexpress LLC (2S)-2-[[3-cyclobutyl-5-(3,4,5-trifluorophenoxy)imidazo[4,5-b]pyridin-2-yl]methylamino]propanamide | 1233231-30-5 | 98.3% | 419.4 g/mol | C20H20F3N5O2 | 25MG

DSP-2230 (ANP-230) is an orally active voltage-gated sodium channel inhibitor used in preclinical research to modulate Nav1.7, Nav1.8, and Nav1.9 activity and to evaluate approaches for neuropathic pain. The compound is supplied as a solid with characterized solubility profiles and storage recommendations for laboratory use only.

Inhibits Nav1.7, Nav1.8, and Nav1.9 with reported IC50s of 7.1 μM, 11.4 μM, and 6.7 μM respectively.
Reported purity 98.33%.
Soluble in DMSO at ≥100 mg/mL; multiple in vivo formulation protocols with solubility ≥2.25 mg/mL are provided.
Powder stability: -20°C for up to 3 years; solution stability conditions are reported.
Intended for preclinical studies of sodium channel pharmacology and neuropathic pain models.

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1,220

Medchemexpress LLC Il-17a antagonist 1 | 2205034-18-8 | MFCD32693918 | 99.7% | 604.71 | C33H41FN6O4 | 10 MG

IL-17A antagonist 1 is a small-molecule antagonist of interleukin-17A used for biochemical and cellular research. It binds IL-17A with a reported Kd of 0.66 μM and shows inhibitory activity against IL-17A (IC50 1.14 nM). In cellular assays it reduces IL-8 production in human keratinocytes (cellular IC50 > 10 μM). Typical applications include target validation and pathway studies.

Small-molecule IL-17A antagonist for research applications.
Biochemical affinity: Kd 0.66 μM.
Potent inhibitory activity: IC50 1.14 nM against IL-17A.
Cellular activity: inhibits IL-8 production in keratinocytes (IC50 > 10 μM).
High purity suitable for biochemical and cellular assays.
Available in multiple package sizes and solution formats for flexibility.
Recommended storage for powder and solutions to preserve stability.

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1,221

eMolecules 4-(4-Bromophenyl)morpholine, HCl | 1186663-63-7 | MFCD12828695 | 1g

Combi-Blocks | 4-(4-Bromophenyl)morpholine, HCl | 1g | 253010382 | ST-1446 | 98.000 | 1186663-63-7 | MFCD12828695 | 278.570 | C10H13BrClNO

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1,222

eMolecules ChemScene / 1-(3-Bromophenyl)-1H-imidazole-4-carboxylic acid / 100mg / 714102785 / CS-0202251 / 0.000 / 445303-24-2 / MFCD16666929 / 267.082 / C10H7BrN2O2

ChemScene / 1-(3-Bromophenyl)-1H-imidazole-4-carboxylic acid / 100mg / 714102785 / CS-0202251 / 0.000 / 445303-24-2 / MFCD16666929 / 267.082 / C10H7BrN2O2

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1,223

Medchemexpress LLC 5-chloro-2-(4-chlorophenyl)-4-methyl-6-(3-(piperidin-1-yl)propoxy)pyrimidine | 1639220-19-1 | 98.6% | 380.31 | C19H23Cl2N3O | 10MG

Sigma-1 receptor antagonist 1 is a potent, selective antagonist of the sigma-1 (σ1) receptor used in preclinical pharmacology and neuropathic pain research. The compound is supplied as a light yellow solid with high chemical purity and is characterized by the molecular formula C19H23Cl2N3O and molecular weight 380.31.

Potent, selective sigma-1 receptor antagonist (Ki = 1.06 nM).
Exhibits antineuropathic pain activity in preclinical models.
High purity: 98.6%.
Solid, light yellow to yellow appearance for easy handling.
Molecular formula C19H23Cl2N3O; molecular weight 380.31.
Supplied in small research sizes suitable for in vitro and in vivo studies.

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1,224

eMolecules 4-(4-Bromophenyl)-2-methylthiazole | 66047-74-3 | MFCD00098207 | 1g

Combi-Blocks | 4-(4-Bromophenyl)-2-methylthiazole | 1g | 205409852 | SH-5232 | 98.000 | 66047-74-3 | MFCD00098207 | 254.150 | C10H8BrNS

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1,225

eMolecules 4-BROMOBENZENEBORONIC ACI 100G

5000165114 4-BROMOBENZENEBORONIC ACI 100G

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1,226

Medchemexpress LLC HY-101785 100mg Medchemexpress, eIF4A3-IN-2 CAS:2095677-20-4 Purity:>98%

Medchemexpress, HY-101785 100mg eIF4A3-IN-2 CAS:2095677-20-4 eIF4A3-IN-2 is a highly selective and noncompetitive eukaryotic initiation factor 4A-3 (eIF4A3) inhibitor with an IC 50 of 110 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.

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1,227

eMolecules N-(4-Bromophenyl)ethanesulfonamide | 57616-20-3 | MFCD01364790 | 1g

Combi-Blocks | N-(4-Bromophenyl)ethanesulfonamide | 1g | 439372363 | LD-2397 | 97.000 | 57616-20-3 | MFCD01364790 | 264.140 | C8H10BrNO2S

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1,228

Medchemexpress LLC HY-15136 5mg Medchemexpress, Lonafarnib CAS:193275-84-2 Purity:>98%

Medchemexpress, HY-15136 5mg Lonafarnib CAS:193275-84-2 Lonafarnib is an orally bioavailable farnesyl protein transferase (FPTase) inhibitor for H-ras, K-ras and N-ras with IC50 of 1.9 nM, 5.2 nM and 2.8 nM, respectively. Lonafarnib has anti-hepatitis delta virus (HDV) activities. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.

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1,229

Medchemexpress LLC 4-isothiazolecarboxamide, 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-(pyrrolidinylbutyl)amino trifluoroacetate | 2805804-54-8 | 98.0% | C22H25BrF5N5O5S | 10MG

CP-547632 TFA is an orally active, ATP-competitive inhibitor of VEGFR-2 and FGF kinases with potent enzymatic activity (IC50 ≈ 11 nM for VEGFR-2 and ≈ 9 nM for FGF). Supplied as the trifluoroacetate (TFA) salt for research use, it has demonstrated antitumor efficacy in xenograft models and is characterized by comprehensive analytical documentation.

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1,230

eMolecules 3-Bromo-5-(trifluoromethoxy)benzene-1,2-diamine | 1191922-50-5 | MFCD00042191 | 1g

Apollo Scientific | 3-Bromo-5-(trifluoromethoxy)benzene-1,2-diamine | 1g | 562457073 | PC48404 | | 1191922-50-5 | MFCD00042191 | 271.037 | C7H6BrF3N2O

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Bromobenzenes

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Chemscene ChemScene | 2,6-Dibromo-4-fluorobenzonitrile | 5G | CS-0161492 | 0.98 | 404928-18-3| MFCD24387472 | 278.91 Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC (2S)-2-[[3-cyclobutyl-5-(3,4,5-trifluorophenoxy)imidazo[4,5-b]pyridin-2-yl]methylamino]propanamide | 1233231-30-5 | 98.3% | 419.4 g/mol | C20H20F3N5O2 | 25MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Il-17a antagonist 1 | 2205034-18-8 | MFCD32693918 | 99.7% | 604.71 | C33H41FN6O4 | 10 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC 5-chloro-2-(4-chlorophenyl)-4-methyl-6-(3-(piperidin-1-yl)propoxy)pyrimidine | 1639220-19-1 | 98.6% | 380.31 | C19H23Cl2N3O | 10MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC HY-15136 5mg Medchemexpress, Lonafarnib CAS:193275-84-2 Purity:>98% Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC 4-isothiazolecarboxamide, 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-(pyrrolidinylbutyl)amino trifluoroacetate | 2805804-54-8 | 98.0% | C22H25BrF5N5O5S | 10MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More