Bromochloromethane(BCM) - ≥98% , CAS No.74-97-5

CAS: 74-97-5 Cat. No.: B105793 Formule: CH₂BrCL Poids moléculaire: 129.38 Beilstein Registry Number: 1730801 Numéro CE: 200-826-3

GRADE & PURITY ≥98%

Synonyms

Methylene Bromochloride | UN 1887 | SCHEMBL49877 | Bromochloromethane 100 microg/mL in Methanol | NCGC00091237-02 | 4-01-00-00074 (Beilstein Handbook Reference) | Q421751 | BRN 1730801 | bromo(chloro)methane | CHLOROBROMOMETHANE | B0573 | SCHEMBL435277 |

Storage

Protected from light,Room temperature

Shipped In

FedEx DG Service

Vue d’ensemble

It has a special sweet taste and is slightly soluble in water. Its solubility in water is 9 g/l in water (20 ° C) and it is miscible with most conventional organic solvents. Non flammable, non explosive, with a low freezing point. Bromochloromethane is an intermediate used in pharmaceuticals, pesticides, fungicides, water treatment agents, and other industries.

Specifications

Synonymes

Methylene Bromochloride | UN 1887 | SCHEMBL49877 | Bromochloromethane 100 microg/mL in Methanol | NCGC00091237-02 | 4-01-00-00074 (Beilstein Handbook Reference) | Q421751 | BRN 1730801 | bromo(chloro)methane | CHLOROBROMOMETHANE | B0573 | SCHEMBL435277 |

Spécifications et pureté

≥98%

Conditions de stockage de stockage

Protected from light,Room temperature

Expédié en

FedEx DG Service

Pureté

≥98%

Noms et identifiants

• Pubchem Sid: 504751067
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751067
• Sourires canoniques: C(Cl)Br
• IUPAC Name: bromo(chloro)methane
• InChIKey: JPOXNPPZZKNXOV-UHFFFAOYSA-N
• INCHI: 1S/CH2BrCl/c2-1-3/h1H2
• Isomères SMILES: C(Cl)Br
• WGK Allemagne: 2
• RTECS: PA5250000
• Numéro ONU: 1887
• Groupe d'emballage: III
• Poids moléculaire: 129.38
• Beilstein: 1730801
• Reaxy-Rn: 1730801
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1730801&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Classe: Alkyl halides
• Subclass: Halomethanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Halomethanes
• Alternative Parents: Organochlorides Organobromides Hydrocarbon derivatives Alkyl chlorides Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Halomethane - Hydrocarbon derivative - Organochloride - Organobromide - Alkyl chloride - Alkyl bromide - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as halomethanes. These are organic compounds in which at least one of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms.
• External Descriptors: an organic chloride - a bromide

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

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Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Light sensitive
• Indice de réfraction: 1.482
• Point d'éclair (°F): 312.8 °F
• Point d'éclair (°C): 156 °C
• Point d'ébullition (°C): 68°C
• Point de fusion (°C): -88°C
• Poids moléculaire: 129.380 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 127.903 Da
• Monoisotopic Mass: 127.903 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 3
• Formal Charge: 0
• Complexity: 4.800
• 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

Références

1. Meng-Meng Lun, Chang-Yuan Su, Jie Li, Qiang-Qiang Jia, Hai-Feng Lu, Da-Wei Fu, Yi Zhang, Zhi-Xu Zhang.  (2023)  Introducing Ferroelasticity into 1D Hybrid Lead Halide Semiconductor by Halogen Substitution Strategy.  Small,  19  (49): (2303127).  [PMID:37625019] [10.1002/smll.202303127]

2. Meng-Meng Lun, Fo-Ling Zhou, Da-Wei Fu, Qiong Ye.  (2022)  Multi-functional hybrid perovskites with triple-channel switches and optical properties.  Journal of Materials Chemistry C,  10  (31): (11371-11378).  [PMID:] [10.1039/D2TC01063A]

3. Yu-Xiang Yang, Chun-Long Mu, Zhen Luo, Wei-Yun Zhu.  (2016)  Bromochloromethane, a Methane Analogue, Affects the Microbiota and Metabolic Profiles of the Rat Gastrointestinal Tract.  APPLIED AND ENVIRONMENTAL MICROBIOLOGY,  82  (3):   [PMID:26567308] [10.1128/AEM.03174-15]

4. Zhi-Jie Wang, Ming-Jing Shen, Zhi-Peng Rao, Pei-Zhi Huang, Meng-Meng Lun, Bo-Wen Deng, Jun-Yi Li, Chang-Feng Wang, Hai-Feng Lu, Da-Wei Fu, Yi Zhang.  (2024)  Structural phase transition drives outright photoluminescence quenching and dielectric duple bistable switching.  Inorganic Chemistry Frontiers,      [PMID:] [10.1039/D4QI00303A]