2-Bromophenol - ≥99%, used for 2-Bromophenol was used in the preparation of anti-benzofurobenzofuran diimides. It was also used to study the photodegradation of 2-bromophenol using UV-Vis spectroscopy and HPLC. various applications , CAS No.95-56-7

CAS: 95-56-7 Cat. No.: B109688 Formula: C₆H₅OBr Peso molecolare: 173.01 Beilstein Registry Number: 1905115 Numero EC: 202-432-7

QUALITÀ & PUREZZA ≥99%

Synonyms

A845333 | DTXSID8052641 | o-Bromophenol | o-bromo-phenol | UNII-A0UB206YF0 | BROMOPHENOL | bromo-phenol | PS-5410 | WLN: QR BE | 2BR | InChI=1/C6H5BrO/c7-5-3-1-2-4-6(5)8/h1-4,8 | O-BROMOPHENOL [MI] | AC-10760 | EINECS 202-432-7 | DTXCID5031214 | SCHEMBL49

Storage

Protected from light,Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifiche

Sinonimi

A845333 | DTXSID8052641 | o-Bromophenol | o-bromo-phenol | UNII-A0UB206YF0 | BROMOPHENOL | bromo-phenol | PS-5410 | WLN: QR BE | 2BR | InChI=1/C6H5BrO/c7-5-3-1-2-4-6(5)8/h1-4,8 | O-BROMOPHENOL [MI] | AC-10760 | EINECS 202-432-7 | DTXCID5031214 | SCHEMBL49

Specifiche e purezza

≥99%

Applicazione

2-Bromophenol was used in the preparation of anti-benzofurobenzofuran diimides. It was also used to study the photodegradation of 2-bromophenol using UV-Vis spectroscopy and HPLC.

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

FedEx DG Service

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

488180351

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180351

Sorrisi canonici

C1=CC=C(C(=C1)O)Br

IUPAC Name

2-bromophenol

InChIKey

VADKRMSMGWJZCF-UHFFFAOYSA-N

INCHI

1S/C6H5BrO/c7-5-3-1-2-4-6(5)8/h1-4,8H

Isomeri SMILES

C1=CC=C(C(=C1)O)Br

WGK Germania

3

RTECS

SJ7875000

Numero UN

1993

Peso molecolare

173.01

Beilstein

1905115

Reaxy-Rn

1905115

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1905115&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Phenols
      • Subclass Halophenols
        • Level5 Bromophenols
          • Level6 O-bromophenols

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Phenols
• Subclass: Halophenols
• Intermediate Tree Nodes: Bromophenols
• Direct Parent: O-bromophenols
• Alternative Parents: Bromobenzenes 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Aryl bromides Organooxygen compounds Organobromides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: 2-bromophenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Halobenzene - Bromobenzene - Monocyclic benzene moiety - Aryl halide - Aryl bromide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as o-bromophenols. These are bromophenols carrying a iodine at the C2 position of the benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

ALOX12 Tchem Arachidonate 12-lipoxygenase (3262 Activities)

Discover Target: ALOX12

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

Discover Target: ALOX15

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

Staphylococcus aureus (210822 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

L1210 (27553 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

norA Quinolone resistance protein norA (2171 Activities)

Discover Target: norA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in chloroform and ether. Slightly soluble in water
• Sensibilità: air sensitive，light sensitive
• Indice di rifrazione: 1.588-1.59
• Punto di infiammabilità (°F): 107.6 °F
• Punto di infiammabilità (°C): 42℃
• Punto di ebollizione (°C): 195°C
• Punto di fusione (°C): 5°C
• Peso molecolare: 173.010 g/mol
• XLogP3: 2.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 171.952 Da
• Monoisotopic Mass: 171.952 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 74.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1