3-Bromo-5-chlorosalicylaldehyde - ≥98% , CAS No.19652-32-5

CAS: 19652-32-5 Cat. No.: B113803 Peso molecular: 235.46 Número EC: 606-351-1
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
3-Bromo-5-chloro-2-hydroxybenzaldehyde | 3-Bromo-5-chloro-2-hydroxy-benzaldehyde | Ractopamine hydrochloride (USP) | D11016 | Benzaldehyde, 3-bromo-5-chloro-2-hydroxy- | SCHEMBL264863 | Z979493248 | FT-0658883 | US8614253, .3-41 | MFCD00051690 | 3-Bromo-5
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
B113803-1g
5

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
5g
B113803-5g
3

10,90US$

16,90US$
Guardar 6,00 US$ (35.50%)
25g
B113803-25g
9

31,90US$

47,90US$
Guardar 16,00 US$ (33.40%)
100g
B113803-100g
3

106,90US$

160,90US$
Guardar 54,00 US$ (33.56%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

3-Bromo-5-chlorosalicylaldehyde is a substituted salicyladehyde.

3-Bromo-5-chlorosalicylaldehyde may be used in the synthesis of the following Schiff base compounds:

· 2-bromo-4-chloro-6-[(E)-o-tolyl-imino-meth-yl]phenol

· 2-bromo-4-chloro-6-[(1-phenyl-ethyl)-imino-meth-yl]phenol

· 2-bromo-4-chloro-6-[(E)-(2-chloro-phen-yl)imino-meth-yl]phenol

· 2′-(3-bromo-5-chloro-2-hydroxy-benzyl-idene)isonicotinohydrazide methanol solvate

Specifications

Sinónimos
3-Bromo-5-chloro-2-hydroxybenzaldehyde | 3-Bromo-5-chloro-2-hydroxy-benzaldehyde | Ractopamine hydrochloride (USP) | D11016 | Benzaldehyde, 3-bromo-5-chloro-2-hydroxy- | SCHEMBL264863 | Z979493248 | FT-0658883 | US8614253, .3-41 | MFCD00051690 | 3-Bromo-5
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488190030
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488190030
Sonrisas canónicasC1=C(C=C(C(=C1C=O)O)Br)Cl
IUPAC Name3-bromo-5-chloro-2-hydroxybenzaldehyde
InChIKeyKNOYZLVIXXBBIB-UHFFFAOYSA-N
INCHI1S/C7H4BrClO2/c8-6-2-5(9)1-4(3-10)7(6)11/h1-3,11H
Isómeros SMILES C1=C(C=C(C(=C1C=O)O)Br)Cl
WGK Alemania 3
Peso molecular 235.46
Reaxy-Rn 2362159
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2362159&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
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbonyl compounds
Intermediate Tree Nodes Aldehydes - Aryl-aldehydes - Benzaldehydes
Direct ParentHydroxybenzaldehydes
Alternative Parents P-chlorophenols  O-bromophenols  Benzoyl derivatives  Chlorobenzenes  Bromobenzenes  Aryl chlorides  Aryl bromides  Vinylogous acids  Organochlorides  Organobromides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Hydroxybenzaldehyde - Benzoyl - 4-halophenol - 2-halophenol - 2-bromophenol - 4-chlorophenol - Halobenzene - Chlorobenzene - Bromobenzene - Phenol - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Aryl bromide - Benzenoid - Vinylogous acid - Organochloride - Organobromide - Organohalogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

8 results found

Lot NumberCertificate TypeFechaArticulo
J2229018Certificate of AnalysisMay 09, 2026 B113803
J2229073Certificate of AnalysisMay 09, 2026 B113803
J2229096Certificate of AnalysisMay 09, 2026 B113803
D2403185Certificate of AnalysisJan 19, 2026 B113803
D2403186Certificate of AnalysisJan 19, 2026 B113803
C2310787Certificate of AnalysisDec 09, 2024 B113803
A1805025Certificate of AnalysisMay 09, 2023 B113803
A1805024Certificate of AnalysisMay 09, 2023 B113803
Propiedades químicas y físicas
Sensibilidadair sensitive ;Moisture sensitive
Punto de fusión (°C)84-88°C
Peso molecular235.460 g/mol
XLogP32.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass233.908 Da
Monoisotopic Mass233.908 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count11
Formal Charge0
Complexity153.000
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
Citations of This Product
Referencias
1. Yan Bao, Lu Gao, Pei Han, Feng Liu, Junbing Zhou, Wenbo Zhang.  (2024)  Multi-color photochromic waterborne polyurethane with high color fastness from hydroxyl-functionalized trichromatic spiropyrans.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2024.112577]
2. Liang Jiao, Meifen Huang, Jiajun Xu, Qiuling Yang, Qiong Wu.  (2024)  Two halogenated coplanar Schiff base complexes: Insights into the impact of halogen substitution on intermolecular interactions via theoretical calculations.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2024.138676]
Calculadoras de soluciones
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