Benzalkonium chloride

Learn More at the Professor and Product Portal of Professor Bruce Lipshutz. Application Phenol protecting group in the synthesis of laterifluorones.

2-(Trimethylsilyl)ethoxymethyl chloride (SEM-Cl) is a widely used reagent for the preparation protection groups for amines, alcohols, phenols, and carboxy groups. The nitrogen of amides and sulfonamides groups are also protected by using SEM-Cl

2-(Trimethylsilyl)ethoxymethyl chloride (SEM-Cl) is a widely used reagent for the preparation protection groups for amines, alcohols, phenols, and carboxy groups. The nitrogen of amides and sulfonamides groups are also protected by using SEM-Cl

2-Benzyl-2，7-diazaspiro[4.4]nonane-1，3-dione hydrochloride.

2-Benzyl-2，7-diazaspiro[4.4]nonane-1，3-dione hydrochloride.

2-Benzyloxybenzoyl chloride

2-Cyano-5-methoxybenzene-1-sulfonyl chloride.

2-Cyano-5-methoxybenzene-1-sulfonyl chloride.

Synonyms: D-ß-HomoPhe(2-CN)-OH·HCl(R)-3-Amino-4-(2-cyanophenyl)butyric acid hydrochloride Purity Limit: &ge 98% (HPLC) CAS No.: 269726-79-6 Molecular Formula: C11H12N2O2·HCl Molecular Weight: 240.

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-Cyanoethyl ether

Application 2-Iodobenzyl chloride was used in the synthesis of: succinimido[3,4-b]indane 1,2,3,4,5,6-hexahydro-1,5-methano-3-benzazocine-2,4-dione 1-(2-iodobenzyi)-1,1-diethylamine 1-(2-iodobenzyl)pyrrolidine 1-(2-iodobenzyl)piperidine