Chlorisondamine chloride

Application Acid labile resin used in Fmoc-based solid phase peptide synthesis. Mild acidic cleavage conditions lead to the release of the peptide acid where fully protected peptides can be released if desired.

Application Acid labile resin used in Fmoc-based solid phase peptide synthesis. Mild acidic cleavage conditions lead to the release of the peptide acid where fully protected peptides can be released if desired.

Application Acid labile resin used in Fmoc-based solid phase peptide synthesis. Mild acidic cleavage conditions lead to the release of the peptide acid where fully protected peptides can be released if desired.

Application Acid labile resin used in Fmoc-based solid phase peptide synthesis. Mild acidic cleavage conditions lead to the release of the peptide acid where fully protected peptides can be released if desired.

2-Methylbenzyl chloride

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.

The kinetic resolution of racemic 2-phenylbutyryl chloride by sterically hindered chiral secondary alcohols has been evaluated. 2-Phenylbutyryl chloride reacts with 4-methoxybenzoyl chloride catalyzed by PdBr(Ph)(PPh 3 ) 2 to yield

The solvolysis of 2-propanesulfonyl chloride by an addition-elimination (association-dissociation) pathway was studied . Application 2-Propanesulfonyl chloride (isopropylsulfonyl chloride) can be used as a reactant to prepare:

The solvolysis of 2-propanesulfonyl chloride by an addition-elimination (association-dissociation) pathway was studied . Application 2-Propanesulfonyl chloride (isopropylsulfonyl chloride) can be used as a reactant to prepare:

The solvolysis of 2-propanesulfonyl chloride by an addition-elimination (association-dissociation) pathway was studied . Application 2-Propanesulfonyl chloride (isopropylsulfonyl chloride) can be used as a reactant to prepare:

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.

3,3-Dimethylacryloyl chloride reacts with silylketene acetals in acetonitrile to give &#948-ethylenic &#946-keto esters . Application 3,3-Dimethylacryloyl chloride was used in the synthesis of: substituted 4,4-dimethyl-3,4-dihydro-1 H