(Bromomethyl)cyclopropane - ≥97% , CAS No.7051-34-5

CAS: 7051-34-5 Cat. No.: B109676 Formula: C₄H₇Br Peso molecolare: 135 Beilstein Registry Number: 605296 Numero EC: 230-331-8

GRADE & PURITY ≥97%

Synonyms

(Bromomethyl)cyclopropane, 97% | cyclopropyl-methylbromide | cyclopropylmethyl-bromide | UNII-D8ZPP7X54B | (BROMO)(CYCLOPROPYL)METHANE | (bromomethyl) cyclopropane | 1-bromomethylcyclopropane | 1-bromomethyl-cyclopropane | bromocyclopropylmethane | bromom

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

The coupling reaction of (bromomethyl)cyclopropane with phenylmagnesium bromide was studied.

(Bromomethyl)cyclopropane is used in the synthesis of 1,4-dienes by iron-catalyzed cross-coupling with alkenyl Grignard reagents. It has been used as a synthetic building block for the introduction of the cyclopropylmethyl group.

Specifications

Sinonimi

(Bromomethyl)cyclopropane, 97% | cyclopropyl-methylbromide | cyclopropylmethyl-bromide | UNII-D8ZPP7X54B | (BROMO)(CYCLOPROPYL)METHANE | (bromomethyl) cyclopropane | 1-bromomethylcyclopropane | 1-bromomethyl-cyclopropane | bromocyclopropylmethane | bromom

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

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: 528753490
• Sorrisi canonici: C1CC1CBr
• IUPAC Name: bromomethylcyclopropane
• InChIKey: AEILLAXRDHDKDY-UHFFFAOYSA-N
• INCHI: 1S/C4H7Br/c5-3-4-1-2-4/h4H,1-3H2
• Isomeri SMILES: C1CC1CBr
• WGK Germania: 3
• Numero UN: 1993
• Peso molecolare: 135
• Beilstein: 605296
• Reaxy-Rn: 605296
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605296&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 homomonocyclic compounds
• Substituents: Hydrocarbon derivative - Organobromide - Alkyl halide - Alkyl bromide - Aliphatic homomonocyclic 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: Not miscible in water.
• Sensibilità: Heat Sensitive
• Indice di rifrazione: 1.475-1.479
• Punto di infiammabilità (°F): 105.8 °F
• Punto di infiammabilità (°C): 41 °C
• Punto di ebollizione (°C): 102-108°C
• Peso molecolare: 135.000 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• 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: 30.600
• 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. Xin Bao, Chunhong Wang, Zhenyu Zhang, Qinghua Cao, Fei Liu, Jing Chen, Chuanzhi Zhang, Haining Na, Jin Zhu.  (2021)  Wet spinning to prepare filaments from three cellulose carbonated derivatives: Synthesis, characterization and filament properties.  Carbohydrate Polymer Technologies and Applications,      [PMID:] [10.1016/j.carpta.2021.100099]