Antipsychotics

Lithium borohydride, a white solid, may be prepared from the exchange reaction of LiCl and sodium borohydride in isopropylamine. The orthorhombic crystal structure converts to tetragonal at 108 o C and eventually melting at 278 o C.

Application Lithium borohydride is a general reducing agent commonly used to reduce aldehydes, ketones esters, lactones, and epoxides. It catalyzes hydroboration of alkenes.

Application Lithium borohydride is a general reducing agent commonly used to reduce aldehydes, ketones esters, lactones, and epoxides. It catalyzes hydroboration of alkenes.

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency.

Application Lithium borohydride solution (2M in THF) has been used for the reduction of 5-benzylidene-2,4-thiazolidinediones and 5-benzylidene-4-oxo-2-thiazolidinethiones to form 5-benzyl-2,4-thiazolidinediones and

Application Lithium borohydride solution (2M in THF) has been used for the reduction of 5-benzylidene-2,4-thiazolidinediones and 5-benzylidene-4-oxo-2-thiazolidinethiones to form 5-benzyl-2,4-thiazolidinediones and

Application Lithium borohydride solution (2M in THF) has been used for the reduction of 5-benzylidene-2,4-thiazolidinediones and 5-benzylidene-4-oxo-2-thiazolidinethiones to form 5-benzyl-2,4-thiazolidinediones and

Application Lithium borohydride solution (2M in THF) has been used for the reduction of 5-benzylidene-2,4-thiazolidinediones and 5-benzylidene-4-oxo-2-thiazolidinethiones to form 5-benzyl-2,4-thiazolidinediones and

Application Lithium borohydride is a commonly used reducing agent. It can also be used a reactant for: Preparation of gallium, indium, rhenium and zinc tris(mercaptoimidazolyl)hydroborato complexes.

LiBr/Chlorotrimethylsilane reagent participates in the conversion of alcohols to bromides. Application Lithium bromide (LiBr) may be employed as a catalyst in the following studies: Transformation of (aromatic- and &#945,&#946-unsaturated)

LiBr/Chlorotrimethylsilane reagent participates in the conversion of alcohols to bromides. Application Lithium bromide (LiBr) may be employed as a catalyst in the following studies: Transformation of (aromatic- and &#945,&#946-unsaturated)

LiBr/Chlorotrimethylsilane reagent participates in the conversion of alcohols to bromides. Application Lithium bromide (LiBr) may be employed as a catalyst in the following studies: Transformation of (aromatic- and &#945,&#946-unsaturated)