Tribrommethan - ≥99%, enthält 1-3% Ethanol als Stabilisator , CAS No.75-25-2

CAS: 75-25-2 Cat. No.: T108556 Summenformel: CHBr₃ Molekulargewicht: 252.73 Beilstein Registry Number: 1731048 EG-Nummer: 200-854-6 PubChem CID: 5558

QUALITÄT & REINHEIT ≥99%, contains 1-3% ethanol as stabilizer

Synonyms

AKOS009031540 | Q409799 | S0653 | DB03054 | FT-0623471 | DTXCID401374 | RCRA Abfallnummer U225 | AT27291 | Methyl tribromide | Tribromomethane 100 microg/mL in Methanol | Bromoform [UN2515] [Poison] | BROMOFORM [WHO-DD] | CHBr3 | J-519947 | Methenyl trib

Storage

Geschützt vor Licht

Shipped In

FedEx DG Service

Übersicht

Bromoform (Tribrommethan) wurde für die Synthese von α-tribrommethylierten N-Sulfonylaminen verwendet.

Spezifikationen

Synonyme

AKOS009031540 | Q409799 | S0653 | DB03054 | FT-0623471 | DTXCID401374 | RCRA Abfallnummer U225 | AT27291 | Methyl tribromide | Tribromomethane 100 microg/mL in Methanol | Bromoform [UN2515] [Poison] | BROMOFORM [WHO-DD] | CHBr3 | J-519947 | Methenyl trib

Spezifikationen & Reinheit

≥99%, enthält 1-3% Ethanol als Stabilisator

Storage

Geschützt vor Licht

Verschickt in

FedEx DG Service

Reinheit

≥99%

Namen und Kennungen

Pubchem Sid

528769114

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528769114

Kanonisches Lächeln

C(Br)(Br)Br

IUPAC Name

bromoform

InChIKey

DIKBFYAXUHHXCS-UHFFFAOYSA-N

INCHI

1S/CHBr3/c2-1(3)4/h1H

Isomere SMILES

C(Br)(Br)Br

WGK Deutschland

3

RTECS

PB5600000

PubChem CID

5558

UN-Nummer

2515

Verpackungsgruppe

III

Molekulargewicht

252.73

Beilstein

1731048

Reaxy-Rn

1731048

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Klasse Alkyl halides
      • Subclass Halomethanes

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Klasse: Alkyl halides
• Subclass: Halomethanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Trihalomethanes
• Alternative Parents: Organobromides Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trihalomethane - Hydrocarbon derivative - Organobromide - Alkyl bromide - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as trihalomethanes. These are organic compounds in which exactly three of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms.
• External Descriptors: one-carbon compound - bromomethanes

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

Zugehörige Ziele (menschlich)

CXCL8 Tchem Interleukin-8 (642 Activities)

Discover Target: CXCL8

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

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

Discover Target: TP53

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Solubility in water: Practically Insoluble; Degree of Solubility in water: 1 g/l 20 °C
• Empfindlichkeit: Light sensitive.
• Brechungsindex: 1.5976
• Siedepunkt (°C): 148-150°C
• Schmelzpunkt (°C): 8-9°C
• Molekulargewicht: 252.730 g/mol
• XLogP3: 2.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 251.761 Da
• Monoisotopic Mass: 249.763 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 8.000
• 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