4-Bromo-1-butene - ≥97% , CAS No.5162-44-7

CAS: 5162-44-7 Cat. No.: B106906 Formula: C₄H₇Br Peso molecolare: 135 Beilstein Registry Number: 1098377 Numero EC: 225-937-4

GRADE & PURITY ≥97%

Synonyms

4-BROMOBUTENE-1 | GEO-00402 | F8880-1792 | J-800293 | Q63392670 | AKOS005166833 | 4-bromo-but-1-ene | 4-Bromobut-1-ene | EINECS 225-937-4 | 4-bromo-1butene | 4-BROMO-1-BUTENE | 4-Bromo-1-butene, stab. with silver | ALLYLCARBINYL BROMIDE | B0920 | FT-06009

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Panoramica

4-Bromo-1-butene has been used in a preparation of dienehydrazides which, in turn, provided cyclic enehydrazides by ring closing metathesis. Double alkylation of lactams, followed by Grubbs ring-closing metathesis, gives access to the bicyclic spiroimine ring system of the bicyclic spiroimine ring system of the biotoxin gymnodimine.

Specifications

Sinonimi

4-BROMOBUTENE-1 | GEO-00402 | F8880-1792 | J-800293 | Q63392670 | AKOS005166833 | 4-bromo-but-1-ene | 4-Bromobut-1-ene | EINECS 225-937-4 | 4-bromo-1butene | 4-BROMO-1-BUTENE | 4-Bromo-1-butene, stab. with silver | ALLYLCARBINYL BROMIDE | B0920 | FT-06009

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 504753030
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753030
• Sorrisi canonici: C=CCCBr
• IUPAC Name: 4-bromobut-1-ene
• InChIKey: DMAYBPBPEUFIHJ-UHFFFAOYSA-N
• INCHI: 1S/C4H7Br/c1-2-3-4-5/h2H,1,3-4H2
• Isomeri SMILES: C=CCCBr
• WGK Germania: 3
• Numero UN: 1993
• Peso molecolare: 135
• Beilstein: 1098377
• Reaxy-Rn: 1098377
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098377&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

Proprietà chimiche e fisiche

• Solubilità: Miscible with water, benzene, ether and ethanol.
• Sensibilità: light sensitive
• Indice di rifrazione: 1.4595-1.4635
• Punto di infiammabilità (°F): 33.8 °F
• Punto di infiammabilità (°C): 1℃
• Punto di ebollizione (°C): 98-100°C
• Peso molecolare: 135.000 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 2
• Exact Mass: 133.973 Da
• Monoisotopic Mass: 133.973 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 24.800
• 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. Xiaofeng Wan, Xiangtai Wei, Jinming Ge, Lingfeng Lu, Ziqiang Liu, Yuanqin Zhu.  (2023)  Towards highly conducting and stable poly(fluorenyl biphenyl)-based anion exchange membranes by grafting dual Y-shaped side-chains.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2023.121760]

2. Mi Wang, Zhenyuan Wang, Jichuan Zhang, Teng Fei, Jiaheng Zhang.  (2023)  Synthesis and properties of bio-renewable ionic salts derived from theophylline as green hypergolic fuels.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2023.121207]

3. Nan Zhao, Xiuxiu Wang, Liru Yao, Huixuan Yan, Ban Qin, Chensha Li, Jianqi Zhang.  (2022)  Actuation performance of a liquid crystalline elastomer composite reinforced by eiderdown fibers.  Soft Matter,  18  (6): (1264-1274).  [PMID:35044410] [10.1039/D1SM01356D]

4. Xiuxiu Wang, Nan Zhao, Ban Qin, Jiaojiao Xu, Wenlong Yang, Chensha Li, Liguo Sun, Jianqi Zhang.  (2020)  Ultrasonics Sonochemistry Assisted Preparation of Polysiloxane Main-Chain Liquid-Crystalline Elastomers.  MACROMOLECULAR CHEMISTRY AND PHYSICS,  221  (11): (2000071).  [PMID:] [10.1002/macp.202000071]

5. Shengbo Zhu, Jin Chigan, Wei Li, Jingyu Yang, Weixing Chen, Wenzhi Zhang, Xiaoling Niu, Xinbing Chen, Zhongwei An.  (2019)  The effect of intermolecular actions on the mesomorphic properties of alkenoxy biphenyl-based liquid crystals.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2019.111880]

6. Ming Li, Ruixia Liu, Qi Liu, Ying Liu, Yifan Liu, Qian Su, Yunong Li, Zifeng Yang.  (2024)  Strategic design and facile synthesis of porous hyper-cross-linked phosphonium bromide microspheres for catalyzing CO2 conversion to cyclic carbonates.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.114306]

7. Yu Fang, Qi Shi, Jinping Qu, Xiang Lu.  (2026)  Single molecule coupling of light and thermal for programmable energy storage.  POLYMER,      [PMID:] [10.1016/j.polymer.2026.129684]