594-51-4 Usage
Appearance
Colorless to pale yellow liquid The compound is a liquid with a color that ranges from colorless to pale yellow.
Odor
Strong, pungent It has a noticeable and irritating smell.
Usage
Reagent in organic synthesis It is commonly used as a reagent in the synthesis of organic compounds.
Applications
Production of pharmaceuticals and agrochemicals 2,3-dibromo-2-methylbutane is used in the manufacturing of various medicines and agricultural chemicals.
Industrial use
Preparation of derivatives for plastics, rubber, and other products It is used to create various derivatives that are used in the production of plastics, rubber, and other industrial products.
Flammability
Highly flammable The chemical is highly susceptible to catching fire and can pose a significant risk.
Health and environmental hazards
Potential hazard to human health and the environment Exposure to 2,3-dibromo-2-methylbutane can be harmful to both humans and the environment.
Handling and storage requirements
Strict requirements Proper handling and storage procedures must be followed to minimize risks associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 594-51-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 594-51:
(5*5)+(4*9)+(3*4)+(2*5)+(1*1)=84
84 % 10 = 4
So 594-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H10Br2/c1-4(6)5(2,3)7/h4H,1-3H3
594-51-4Relevant articles and documents
Andrews,Keefer
, p. 3557,3558 (1953)
Synthesis of 1,1-Dihaloalkanes
Garcia Martinez, A.,Herrera Fernandez, A.,Martinez Alvarez, R.,Garcia Fraile, A.,Bueno Calderon, J.,et al.
, p. 1076 - 1078 (2007/10/02)
The reaction of 1,1-bistrifluoromethylsulfonyloxy-alkanes (2) with magnesium iodide in carbon disulphide at O deg C affords 1,1-diiodoalkanes (3-I) in good yields.No rearrangement products are observed.The reaction of 2 with magnesium bromide in carbon disulphide or titanium tetrachloride in dichloromethane yields either 1,1-dichloro- (3-Cl) or 1,1-dibromoalkanes (3-Br).Rearrangements products are formed from α-branched substrates.
Nucleophilic Contribution of the Solvent in Olefin Bromination. 1. Steric Inhibition to Nucleophilic Solvation in Alkene Bromination via Bromonium Ions
Ruasse, Marie-Francoise,Zhang, Ben-Li
, p. 3207 - 3210 (2007/10/02)
-
