Boc-D-Alaninol

Boc-D-Alaninol (CAS: 106391-86-0) is a high-purity chiral protected amino alcohol fine chemical. This compound features a D-type chiral propanol skeleton with tert-butoxycarbonyl (Boc) protecting group modified on the amino group, possessing stable chemical properties, excellent chiral purity and selective reaction activity. The Boc protecting group effectively avoids amino group side reactions during organic synthesis and can be efficiently deprotected under specific acidic conditions. Boc-D-Alaninol (106391-86-0) is a critical chiral building block, widely applied in peptide synthesis, pharmaceutical chiral intermediate preparation and asymmetric catalytic chemical production.

N-Boc-D-alaninol, Boc-D-Ala-ol, (R) -2- (tert-butoxycarbonylamino) -1-propanol, tert-butyl (R) -1-hydroxypropan-2-ylcarbamate, N-tert-Butoxycarbonyl-D-alaninol

29051990

1. Peptide Synthesis Intermediate Preparation Boc-D-Alaninol (CAS: 106391-86-0) serves as a core protected amino alcohol monomer for standard peptide synthesis processes. Its stable Boc protection structure ensures directional reaction of active hydroxyl groups, effectively avoiding amino group interference and side reactions, supporting high-purity and high-efficiency synthesis of chiral peptide compounds in biochemical fine chemical production. 2. Chiral Pharmaceutical Intermediate Manufacturing Boc-D-Alaninol (106391-86-0) is an essential chiral precursor for the R&D and industrial production of high-end chiral drugs. The single-configurational D-chiral skeleton can optimize the stereoselectivity and pharmacological activity of drug molecules, and is widely used in the customization of anti-inflammatory, antiviral and targeted therapeutic pharmaceutical intermediates. 3. Asymmetric Catalysis Chemical Research Boc-D-Alaninol (CAS: 106391-86-0) can be used as a high-quality chiral auxiliary and chiral ligand source for asymmetric catalytic reactions. Its unique chiral spatial structure provides precise stereochemical induction, improving the enantioselectivity of catalytic reactions, and is widely used in laboratory research and industrial scale-up of asymmetric synthesis processes. 4. Biochemical Fine Chemical Derivatization Boc-D-Alaninol (106391-86-0) supports multi-step selective derivatization of biochemical fine chemicals. The dual active sites of protected amino group and free hydroxyl group enable flexible molecular splicing and structural modification, meeting the customized production needs of various chiral biochemical derivatives.

≥98%

Store at 0 °C in dry, sealed, dark inert environment, avoid high temperature, humid air and strong acid-base conditions to prevent structural decomposition and amino group deprotection

2 years under proper storage

White to off-white crystalline solid

Research Grade, Fine Chemical Grade, Pharmaceutical Intermediate Grade

1.025±0.06 g/cm3

58-61 °C