2,4-Dichloro-5-sulfamoylbenzoic Acid - ≥98%(HPLC)(T) , CAS No.2736-23-4

CAS: 2736-23-4 Cat. No.: D104506 Peso molecular: 270.09 Número EC: 220-358-3
Disponible para pedir
GRADE & PURITY ≥98%(HPLC)(T)
Synonyms
Oprea1_483230 | InChI=1/C7H5Cl2NO4S/c8-4-2-5(9)6(15(10,13)14)1-3(4)7(11)12/h1-2H,(H,11,12)(H2,10,13,14 | Furosemide Imp. B (EP); 2,4-Dichloro-5-sulphamoylbenzoic Acid; Furosemide Impurity B | F1901-0102 | BP-12719 | D2541 | SR-01000537051-1 | ZSHHRBYVHTVR
Storage
Room temperature
Shipped In
Normal
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Size
Estado
Price
Qty
5g
D104506-5g
5

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
25g
D104506-25g
3

11,90US$

17,90US$
Guardar 6,00 US$ (33.52%)
50g
D104506-50g
2

21,90US$

32,90US$
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100g
D104506-100g
1

23,90US$

35,90US$
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250g
D104506-250g
1

52,90US$

79,90US$
Guardar 27,00 US$ (33.79%)
500g
D104506-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

100,90US$

151,90US$
Guardar 51,00 US$ (33.57%)
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Why this grade

≥98%(HPLC)(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Oprea1_483230 | InChI=1/C7H5Cl2NO4S/c8-4-2-5(9)6(15(10, 13)14)1-3(4)7(11)12/h1-2H, (H, 11, 12)(H2, 10, 13, 14 | Furosemide Imp. B (EP); 2, 4-Dichloro-5-sulphamoylbenzoic Acid; Furosemide Impurity B | F1901-0102 | BP-12719 | D2541 | SR-01000537051-1 | ZSHHRBYVHTVR
Especificaciones y pureza
≥98%(HPLC)(T)
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%(HPLC)(T)
Nombres e identificadores
Pubchem Sid488182406
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488182406
Sonrisas canónicasC1=C(C(=CC(=C1S(=O)(=O)N)Cl)Cl)C(=O)O
IUPAC Name2,4-dichloro-5-sulfamoylbenzoic acid
InChIKeyZSHHRBYVHTVRFK-UHFFFAOYSA-N
INCHI1S/C7H5Cl2NO4S/c8-4-2-5(9)6(15(10,13)14)1-3(4)7(11)12/h1-2H,(H,11,12)(H2,10,13,14)
Isómeros SMILES C1=C(C(=CC(=C1S(=O)(=O)N)Cl)Cl)C(=O)O
RTECS DG8100000
Peso molecular 270.09
Reaxy-Rn 2219046
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2219046&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Benzoic acids
Direct ParentDichlorobenzoic acids
Alternative Parents 2-halobenzoic acids  4-halobenzoic acids  Benzenesulfonamides  Halobenzoic acids  Benzenesulfonyl compounds  1-carboxy-2-haloaromatic compounds  Benzoyl derivatives  Dichlorobenzenes  Organosulfonamides  Aryl chlorides  Vinylogous halides  Aminosulfonyl compounds  Monocarboxylic acids and derivatives  Organic nitrogen compounds  Organic oxides  Organochlorides  Organooxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents 2,4-dichlorobenzoic acid - Benzenesulfonamide - 2-halobenzoic acid or derivatives - 4-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - 2-halobenzoic acid - Halobenzoic acid - 4-halobenzoic acid - Benzenesulfonyl group - Benzoyl - 1,3-dichlorobenzene - 1-carboxy-2-haloaromatic compound - Chlorobenzene - Halobenzene - Aryl halide - Organosulfonic acid amide - Aryl chloride - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Vinylogous halide - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organochloride - Organooxygen compound - Organosulfur compound - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organohalogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as dichlorobenzoic acids. These are benzoic acids having two chlorine atoms attached to the carboxylated benzene ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CA5A Tclin Carbonic anhydrase 5A, mitochondrial (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA5B Tclin Carbonic anhydrase 5B, mitochondrial (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA6 Tclin Carbonic anhydrase 6 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA13 Tclin Carbonic anhydrase 13 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA1 Tclin Carbonic anhydrase 1 (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA3 Tclin Carbonic anhydrase 3 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase 2 (5 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA4 Tclin Carbonic anhydrase 4 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA12 Tclin Carbonic anhydrase 12 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA14 Tclin Carbonic anhydrase 14 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA9 Tclin Carbonic anhydrase 9 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA7 Tclin Carbonic anhydrase 7 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

23 results found

Lot NumberCertificate TypeFechaArticulo
I2209056Certificate of AnalysisJun 11, 2026 D104506
I2209055Certificate of AnalysisJun 11, 2026 D104506
I2209054Certificate of AnalysisJun 11, 2026 D104506
I2525572Certificate of AnalysisOct 11, 2025 D104506
I2525559Certificate of AnalysisOct 11, 2025 D104506
J2126709Certificate of AnalysisAug 11, 2025 D104506
J2112169Certificate of AnalysisJul 15, 2025 D104506
J2112167Certificate of AnalysisJul 15, 2025 D104506
J2112166Certificate of AnalysisJul 15, 2025 D104506
J2112165Certificate of AnalysisJul 15, 2025 D104506
I2008181Certificate of AnalysisJul 16, 2024 D104506
D2303779Certificate of AnalysisFeb 18, 2023 D104506
D2303764Certificate of AnalysisFeb 18, 2023 D104506
D2303757Certificate of AnalysisFeb 18, 2023 D104506
D2303751Certificate of AnalysisFeb 18, 2023 D104506
D2303750Certificate of AnalysisFeb 18, 2023 D104506
D2303745Certificate of AnalysisFeb 18, 2023 D104506
D2303743Certificate of AnalysisFeb 18, 2023 D104506
D2303708Certificate of AnalysisFeb 18, 2023 D104506
D2303707Certificate of AnalysisFeb 18, 2023 D104506
D2303706Certificate of AnalysisFeb 18, 2023 D104506
D2303705Certificate of AnalysisFeb 18, 2023 D104506
B2313027Certificate of AnalysisSep 17, 2021 D104506

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Propiedades químicas y físicas
Punto de fusión (°C)230-234°C
Peso molecular270.090 g/mol
XLogP31.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count2
Exact Mass268.932 Da
Monoisotopic Mass268.932 Da
Topological Polar Surface Area106.000 Ų
Heavy Atom Count15
Formal Charge0
Complexity352.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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