Dichlorophenylborane - ≥98%(T) , CAS No.873-51-8

CAS: 873-51-8 Cat. No.: D155799 Formule: C6H5BCl2 Poids moléculaire: 158.82 Beilstein Registry Number: 2243580 Numéro CE: 629-153-7
DISPONIBLE À COMMANDE
GRADE & PURITY ≥98%(T)
Synonyms
Borine, dichlorophenyl- | Phenylboron dibromide | D4367 | InChI=1/C6H5BCl2/c8-7(9)6-4-2-1-3-5-6/h1-5 | phenyldichloroboron | SCHEMBL29602 | FT-0633047 | D90280 | Tri(2-butoxyethanol) phosphate | NSC93889 | UNII-SLG75RQ9B6 | EPA Pesticide Chemical Code 285
Storage
Room temperature,Argon charged
Shipped In
Normal
Size
Allemagne (EU)
USA*
Price
Qty
1g
D155799-1g
4 En stock
51,98€
5g
D155799-5g
3 En stock
190,82€
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Room temperature,Argon charged 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.

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Literature proof

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

Vue d’ensemble

Dichlorophenylborane can be used as a catalyst for: The synthesis of an antiproliferative macrolide and cell migration inhibitor lactimidomycin. Enantioselective synthesis of polyketide segments using vinylogous Mukaiyama aldol reactions. Enantioselective Diels-Alder cycloadditions after its reaction with allo-threonine derivatives. Stereoselective alkylative ring opening of cyclic anhydrides. Cross-metathesis reaction of amino derivatives with olefins. Asymmetric acetate aldol reactions.

Specifications

Synonymes
Borine, dichlorophenyl- | Phenylboron dibromide | D4367 | InChI=1/C6H5BCl2/c8-7(9)6-4-2-1-3-5-6/h1-5 | phenyldichloroboron | SCHEMBL29602 | FT-0633047 | D90280 | Tri(2-butoxyethanol) phosphate | NSC93889 | UNII-SLG75RQ9B6 | EPA Pesticide Chemical Code 285
Spécifications et pureté
≥98%(T)
Conditions de stockage de stockage
Room temperature,Argon charged
Expédié en
Normal
Pureté
≥98%(T)
Noms et identifiants
Pubchem Sid504757087
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504757087
Sourires canoniquesB(C1=CC=CC=C1)(Cl)Cl
IUPAC Namedichloro(phenyl)borane
InChIKeyNCQDQONETMHUMY-UHFFFAOYSA-N
INCHI1S/C6H5BCl2/c8-7(9)6-4-2-1-3-5-6/h1-5H
Isomères SMILES B(C1=CC=CC=C1)(Cl)Cl
WGK Allemagne 3
Poids moléculaire 158.82
Beilstein 2243580
Reaxy-Rn 2243576
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2243576&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
ClasseBenzene and substituted derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzene and substituted derivatives
Alternative Parents Boronic acid derivatives  Organic metalloid salts  Organoboron compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Boronic acid derivative - Organic metalloid salt - Hydrocarbon derivative - Organic salt - Organoboron compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

15 results found

Lot NumberCertificate TypeDateArticle
G2610440Certificate of AnalysisJun 26, 2026 D155799
G2610450Certificate of AnalysisJun 26, 2026 D155799
J2428607Certificate of AnalysisJul 10, 2024 D155799
C2325567Certificate of AnalysisDec 02, 2022 D155799
C2325575Certificate of AnalysisDec 02, 2022 D155799
C2325587Certificate of AnalysisDec 02, 2022 D155799
H2407043Certificate of AnalysisDec 02, 2022 D155799
H2504063Certificate of AnalysisDec 02, 2022 D155799
I2511140Certificate of AnalysisDec 02, 2022 D155799
H2229279Certificate of AnalysisAug 09, 2022 D155799
E2622060Certificate of AnalysisJul 30, 2022 D155799
H2229276Certificate of AnalysisJul 30, 2022 D155799
A2220480Certificate of AnalysisJan 06, 2022 D155799
A2220490Certificate of AnalysisJan 06, 2022 D155799
A2220492Certificate of AnalysisJan 06, 2022 D155799

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Propriétés chimiques et physiques
SolubilitéSoluble in water (Reacts violently).
SensibilitéMoisture sensitive.
Indice de réfraction1.54
Point d'éclair (°F)57°F
Point d'éclair (°C)14°C
Point d'ébullition (°C)175°C
Point de fusion (°C)7°C(lit.)
Poids moléculaire158.820 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass157.986 Da
Monoisotopic Mass157.986 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count9
Formal Charge0
Complexity79.100
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
Calculateurs de solution
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