1-(4-bromofenil)etilammina - ≥98%(GC) , CAS No.24358-62-1

CAS: 24358-62-1 Cat. No.: B151926 Formula: C₈H₁₀BrN Peso molecolare: 200.08 Numero EC: 246-200-3

GRADE & PURITY ≥98%(GC)

Synonyms

3-Bromo-6-chloropyridine | (-)-1-(4-Bromophenyl)ethylamine | AM20060823 | (+/-)-1-(4-BROMOPHENYL)ETHYLAMINE | 4-Bromo- alpha -methylbenzylamine | BBL034684 | FT-0605664 | 4-bromomethylbenzenesulfonyl chloride | B2266 | SY009358 | BCP09414 | H10501 | 1-(4-

Storage

Argon charged,Room temperature

Shipped In

Normale

Specifications

Sinonimi

3-Bromo-6-chloropyridine | (-)-1-(4-Bromophenyl)ethylamine | AM20060823 | (+/-)-1-(4-BROMOPHENYL)ETHYLAMINE | 4-Bromo- alpha -methylbenzylamine | BBL034684 | FT-0605664 | 4-bromomethylbenzenesulfonyl chloride | B2266 | SY009358 | BCP09414 | H10501 | 1-(4-

Specifiche e purezza

≥98%(GC)

Condizioni di conservazione di stoccaggio

Argon charged,Room temperature

Spedito in

Normale

Purezza

≥98%(GC)

Nomi e identificatori

• Pubchem Sid: 504756052
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756052
• Sorrisi canonici: CC(C1=CC=C(C=C1)Br)N
• IUPAC Name: 1-(4-bromophenyl)ethanamine
• InChIKey: SOZMSEPDYJGBEK-UHFFFAOYSA-N
• INCHI: 1S/C8H10BrN/c1-6(10)7-2-4-8(9)5-3-7/h2-6H,10H2,1H3
• Isomeri SMILES: CC(C1=CC=C(C=C1)Br)N
• WGK Germania: 3
• Peso molecolare: 200.08
• Reaxy-Rn: 2412318
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2412318&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Halobenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Halobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Bromobenzenes
• Alternative Parents: Aralkylamines Aryl bromides Organopnictogen compounds Organobromides Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Aralkylamine - Bromobenzene - Aryl halide - Aryl bromide - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organobromide - Organohalogen compound - Primary aliphatic amine - Amine - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as bromobenzenes. These are organic compounds containing a bromine atom attached to a 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

Proprietà chimiche e fisiche

• Sensibilità: air sensitive
• Indice di rifrazione: n20/D 1.566
• Punto di infiammabilità (°F): 235.4 °F
• Punto di infiammabilità (°C): 113 °C
• Peso molecolare: 200.080 g/mol
• XLogP3: 1.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 199 Da
• Monoisotopic Mass: 199 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 97.400
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Jingjing Zhu, Huaqiang Chen, Lan Wang, Engang Fu, Jianping Wu, Qilei Zhang, Lirong Yang, Gang Xu.  (2021)  High-efficient dynamic kinetic resolution of amines with a core-shell hollow mesoporous MIL-101@Pd@ZIF-8 nanocatalyst and lipase.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2021.111490]

2. Tong Li, Hui Li, Jia Chen, Yongliang Yu, Shuai Chen, Jianhua Wang, Hongdeng Qiu.  (2024)  Histidine-modified pillar[5]arene-functionalized mesoporous silica materials for highly selective enantioseparation.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38776604] [10.1016/j.chroma.2024.465011]

3. Siru Ren, Qi Zhang, Song Xue, Siyao Liu, Mengjie Rui.  (2020)  Use of Gamithromycin as a Chiral Selector in Capillary Electrophoresis.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:32327223] [10.1016/j.chroma.2020.461099]