Central nervous system drugs

Synonyms: D-ß-HomoPhe(2-Me)-OH·HCl(R)-3-Amino-4-(2-methylphenyl)butyric acid hydrochloride Purity Limit: &ge 98% (TLC) CAS No.: 269398-79-0 Molecular Formula: C11H15NO2·HCl Molecular Weight: 229.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and 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 rare and 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 rare and 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 rare and 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.

Application Reactant for: Preparation of platinum cyclometalated N-heterocyclic carbene complexes with chiral phosphines as catalysts Preparation of oxoazetidinylbutenyl acetamides via rhodium-catalyzed hydroformylation Preparation of highly

Application 2-Methylanthraquinone may be used in the preparation of potential bioreducible anthraquinone derivatives.

Application 2-Methylanthraquinone may be used in the preparation of potential bioreducible anthraquinone derivatives.

2-Methylbenzhydrol on etherification with tropine yields tropinyl 2-methyl-benzhydryl ether hydrobromide (BS 6825) . It also undergoes reduction in acetic acid containing iodine and aqueous hypophosphorous acid to yield diphenylmethanes .

Application 2-Methylbenzylamine (o-Methylbenzylamine) was used in the preparation of boc-2-alkylanilines: N- (tert-butoxycarbonyl)-1-methylbenzylamine .

Application 2-Methylbenzylamine (o-Methylbenzylamine) was used in the preparation of boc-2-alkylanilines: N- (tert-butoxycarbonyl)-1-methylbenzylamine .