2-Bromopropane - CP, ≥98% , CAS No.75-26-3

CAS: 75-26-3 Cat. No.: B109114 Formula: C₃H₇Br Peso molecolare: 122.99 Beilstein Registry Number: 741852 Numero EC: 200-855-1

GRADE & PURITY CP, ≥98%

Synonyms

NCGC00257910-01 | AKOS000119846 | InChI=1/C3H7Br/c1-3(2)4/h3H,1-2H | NCGC00091451-01 | STL146524 | 1-isopropylbromide | 2-Bromopropane [UN2344] [Flammable liquid] | 2-Bromopropane, purum, >=99.0% (GC) | Isopropylbromide | iso-propylbromide | 2-Bromopropa

Storage

Room temperature

Shipped In

FedEx DG Service

Specifications

Sinonimi

NCGC00257910-01 | AKOS000119846 | InChI=1/C3H7Br/c1-3(2)4/h3H,1-2H | NCGC00091451-01 | STL146524 | 1-isopropylbromide | 2-Bromopropane [UN2344] [Flammable liquid] | 2-Bromopropane, purum, >=99.0% (GC) | Isopropylbromide | iso-propylbromide | 2-Bromopropa

Specifiche e purezza

CP, ≥98%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

FedEx DG Service

Grado

CP

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 488180056
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180056
• Sorrisi canonici: CC(C)Br
• IUPAC Name: 2-bromopropane
• InChIKey: NAMYKGVDVNBCFQ-UHFFFAOYSA-N
• INCHI: 1S/C3H7Br/c1-3(2)4/h3H,1-2H3
• Isomeri SMILES: CC(C)Br
• WGK Germania: 1
• RTECS: TX4111000
• Numero UN: 2344
• Peso molecolare: 122.99
• Beilstein: 741852
• Reaxy-Rn: 741852
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=741852&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Classe Organobromides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Classe: Organobromides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organobromides
• Alternative Parents: Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organobromide - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as organobromides. These are compounds containing a chemical bond between a carbon atom and a bromine atom.
• 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)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

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

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

Discover Target: THRB

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Solubility in water: Practically Insoluble; Degree of Solubility in water: 318 mg/l 20 °C; Miscible with Chloroform,Benzene,Ether,Alcohol
• Indice di rifrazione: 1.4251
• Punto di infiammabilità (°F): 66.2 °F
• Punto di infiammabilità (°C): 19℃
• Punto di ebollizione (°C): 59.38°C
• Punto di fusione (°C): -89°C
• Peso molecolare: 122.990 g/mol
• XLogP3: 1.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 121.973 Da
• Monoisotopic Mass: 121.973 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 10.800
• 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

Riferimenti

1. Zhong ZhenHua, Chen YuPing, Xia HongYing, Chen ZhenZhen, Cheng QiZhen.  (2021)  Development and Validation of a Sensitive GC–MS/MS Method for the Determination of Five Potential Genotoxic Impurities in Abiraterone Acetate.  JOURNAL OF CHROMATOGRAPHIC SCIENCE,  60  (2): (105-110).  [PMID:34059885] [10.1093/chromsci/bmab052]

2. Dan He, Ying Wu, Zhengping Liu, Tuo Zhao.  (2017)  The synthesis of poly(phenylene sulfide sulfone) in ionic liquids at atmospheric pressure.  RSC Advances,  7  (63): (39604-39610).  [PMID:] [10.1039/C7RA04627H]

3. Li Yongqiang, Yang Siwei, Bao Wancheng, Tao Quan, Jiang Xiuyun, Li Jipeng, He Peng, Wang Gang, Qi Kai, Dong Hui, Ding Guqiao, Xie Xiaoming.  (2024)  Accelerated proton dissociation in an excited state induces superacidic microenvironments around graphene quantum dots.  Nature Communications,  15  (1): (1-13).  [PMID:39103388] [10.1038/s41467-024-50982-x]

4. Ting Xu, Zihan Xue, Xinhui Li, Miaomiao Zhang, Ruige Yang, Shangshang Qin, Yong Guo.  (2025)  Development of Membrane-Targeting Osthole Derivatives Containing Pyridinium Quaternary Ammonium Moieties with Potent Anti-Methicillin-Resistant Staphylococcus aureus Properties.  JOURNAL OF MEDICINAL CHEMISTRY,      [PMID:40205941] [10.1021/acs.jmedchem.4c03167]