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

CAS: 7051-34-5 Cat. No.: B109676 Formule: C₄H₇Br Poids moléculaire: 135 Beilstein Registry Number: 605296 Numéro CE: 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

Vue d’ensemble

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

Synonymes

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

Spécifications et pureté

≥97%

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥97%

Noms et identifiants

Pubchem Sid

528753490

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528753490

Sourires canoniques

C1CC1CBr

IUPAC Name

bromomethylcyclopropane

InChIKey

AEILLAXRDHDKDY-UHFFFAOYSA-N

INCHI

1S/C4H7Br/c5-3-4-1-2-4/h4H,1-3H2

Isomères SMILES

C1CC1CBr

WGK Allemagne

3

Numéro ONU

1993

Poids moléculaire

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
• Description: 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

Propriétés chimiques et physiques

• Solubilité: Not miscible in water.
• Sensibilité: Heat Sensitive
• Indice de réfraction: 1.475-1.479
• Point d'éclair (°F): 105.8 °F
• Point d'éclair (°C): 41 °C
• Point d'ébullition (°C): 102-108°C
• Poids moléculaire: 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