Chloroform-Isoamyl Alcohol

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.

Application 2-Chlorophenethyl alcohol may be used in the chemical synthesis of amines.

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.

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-Chloro-4-hydroxyphenylacetic acid is an auxin influx inhibitor . It is one of the major chlorinated metabolite of chlorotyrosine .

3-Chloro-4-methoxybenzyl alcohol

3-Chlorophenethyl alcohol undergoes coupling reaction with dibutylamine .

Synonyms: D-ß-HomoPhe(3-Me)-OH·HCl(R)-3-Amino-4-(3-methylphenyl)butyric acid hydrochloride Purity Limit: &ge 99% (HPLC) CAS No.: 269398-82-5 Molecular Formula: C11H16ClNO2 Molecular Weight: 229.

Synonyms: D-ß-HomoPhe(3-Me)-OH·HCl(R)-3-Amino-4-(3-methylphenyl)butyric acid hydrochloride Purity Limit: &ge 99% (HPLC) CAS No.: 269398-82-5 Molecular Formula: C11H16ClNO2 Molecular Weight: 229.

Synonyms: D-ß-HomoPhe(3-Me)-OH·HCl(R)-3-Amino-4-(3-methylphenyl)butyric acid hydrochloride Purity Limit: &ge 99% (HPLC) CAS No.: 269398-82-5 Molecular Formula: C11H16ClNO2 Molecular Weight: 229.

Application 4,5-Dimethoxy-2-nitrobenzyl chloroformate (NVOC-Cl) is a photolabile protecting reagent, commonly used in peptide or nucleotide synthesis to protect amines and hydroxyl groups. General applications are: Preparation of inactive, caged

4-Chloro-1-naphthol is a substrate for HRP in a reaction that results in a colored precipitate. It is commonly used for colorimetric detection and visualization of proteins in western blotting.