10601-61-3

Basic information

• Product Name: 1-bromo-2-chloro-2-methylpropane
• Synonyms: 1-bromo-2-chloro-2-methylpropane;Einecs 234-222-6
• CAS NO: 10601-61-3
• Molecular Formula: C₄H₈BrCl
• Molecular Weight: 171.46332
• EINECS: 234-222-6
• Mol File: 10601-61-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 129.5°Cat760mmHg
• Flash Point: 45.2°C
• Appearance: /
• Density: 1.438g/cm³
• Vapor Pressure: 12.4mmHg at 25°C
• Refractive Index: 1.467
• CAS DataBase Reference: 1-bromo-2-chloro-2-methylpropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2-chloro-2-methylpropane(10601-61-3)
• EPA Substance Registry System: 1-bromo-2-chloro-2-methylpropane(10601-61-3)

Safety Data

• Hazardous Substances Data: 10601-61-3(Hazardous Substances Data)

Usage

General Description

1-bromo-2-chloro-2-methylpropane is a chemical compound with the molecular formula C4H8BrCl. It is a colorless liquid that is flammable and has a strong, unpleasant odor. Also known as tert-butyl bromochloride, this compound is commonly used as an alkylating agent in chemical reactions. It is classified as a halogenated hydrocarbon and is primarily used in organic synthesis as a reagent for the introduction of the tert-butyl group into organic compounds. It is important to handle 1-bromo-2-chloro-2-methylpropane with care, as it is a hazardous substance that can cause irritation to the skin, eyes, and respiratory system, and may be harmful if ingested or inhaled.

InChI:InChI=1/C4H8BrCl/c1-4(2,6)3-5/h3H2,1-2H3

Upstream product

• 115-11-7 isobutene 
• 594-34-3 1,2-dibromo-2-methyl-propane 
• 507-20-0 tertiary butyl chloride 

Relevant articles and documents

BiX3 as an efficient and selective reagent for the halogen exchange reaction

Bismuth halides are efficient and selective reagents in the halogen exchange reactions carried out under mild conditions. This rapid, high yield reaction proceeds mainly with retention of configuration.

SELECTIVITIES OF pi - AND sigma -SUCCINIMIDYL RADICALS IN SUBSTITUTION AND ADDITION REACTIONS. APPENDIX: RESPONSE TO WALLING, EL-TALIAWI, AND ZHAO.

A new method for studies of pi -succinimidyl (S// pi ) radicals is described, one that makes possible the study of reactions of this radical with a variety of substrates not accessible by the use of Br//2-NBS. NBS systems containing BrCCl//3 at mole fractions greater than 0. 3 show all the characteristics associated with S// pi behavior, and they function in the presence of olefins which serve as Br//2 scavengers. If CCl//4 is substituted for BrCCl//3, the system is clearly S// sigma . The S// pi behavior is contrasted with S// sigma and Br multiplied by (times) reactivities for H abstractions from a variety of substrates and for additions to tert-butylethylene, isobutylene, and 1,3-butadiene. In early-transition-state systems, for H transfer, the strength of the bond being broken and the strength of the bond being made are not the major factors in determining reactivities. The behavior in late-transition-state systems is influenced by both bond strengths. The S// pi radical shows intermediate behavior. These conclusions are supported by primary deuterium isotope effects for methylene chloride and chlororoform. The Appendix addresses a number of questions raised by the preliminary study of NBS reactions by Walling et al.