Bromamide

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

2-Bromobenzyl bromide is a reagent used to protect ketones and aldehydes in their less reactive alcohol oxidation states and as a coupling component in various reactions. Application 2-Bromobenzyl bromide was used in the synthesis of: substituted

2-Bromobenzyl bromide is a reagent used to protect ketones and aldehydes in their less reactive alcohol oxidation states and as a coupling component in various reactions. Application 2-Bromobenzyl bromide was used in the synthesis of: substituted

Analysis Note Assay (argentometric): &#8805 99.0 % Melting range (lower value): &#8805 171 &#176C Melting range (upper value): &#8804 176 &#176C Identity (IR): passes test

Analysis Note Assay (argentometric): &#8805 99.0 % Melting range (lower value): &#8805 171 &#176C Melting range (upper value): &#8804 176 &#176C Identity (IR): passes test

2-Methylbenzyl bromide

3-Bromobenzyl bromide undergoes reduction with diethylzinc in the presence of Pd(PPh 3 ) 4 to yield corresponding hydrocarbon . Application 3-Bromobenzyl bromide was used in the synthesis of: 1,7-di(3-bromobenzyl)cyclen substituted 8-arylquinoline,

3-Bromobenzyl bromide undergoes reduction with diethylzinc in the presence of Pd(PPh 3 ) 4 to yield corresponding hydrocarbon . Application 3-Bromobenzyl bromide was used in the synthesis of: 1,7-di(3-bromobenzyl)cyclen substituted 8-arylquinoline,

3-Methylbenzyl bromide

Application 4-Bromobenzyl bromide was used to prepare a 20-member aminomethyl-substituted biaryl library via sequential N-alkylation of various amines .

Application 4-Bromobenzyl bromide was used to prepare a 20-member aminomethyl-substituted biaryl library via sequential N-alkylation of various amines .

4-Methylbenzyl bromide