N-Boc-L-Alaninol

Product Details

CAS No:79069-13-9

MF:C8H17NO3

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:Tons

Synonyms:N-tert-Butoxycarbonyl-L-alaninol; N-boc-l-alanine alcohol;N-BOC-S-ALANINOL;N-ALPHA-T-BOC-L-ALANINOL;N-ALPHA-TERT-BUTYLOXYCARBONYL-L-ALANINOL;N-T-BUTOXYCARBONYL-L-ALANINOL;N-T-BOC-L-ALANINOL;Boc-Ala-ol~(S)-2-(Boc-amino)-1-propanol~N-(tert-Butoxycarbonyl)-L-alaninol;Butoxycarbonylalaninol,"1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamate","1,1-Dimethylethyl N-[(1S)-2-hydroxy-1-methylethyl]carbamate; 1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamate; Boc-L-alaninol; 79069-13-9; N-Boc-L-alaninol; Boc-Alaninol; (S)-2-(Boc-amino)-1-propanol; (S)-tert-Butyl (1-hydroxypropan-2-yl)carbamate; MFCD00043121; tert-butyl N-[(2S)-1-hydroxypropan-2-yl]carbamate; N-(tert-Butoxycarbonyl)-L-alaninol; (S)-N-BOC-alaninol; (S)-2-(tert-Butoxycarbonylamino)-1-propanol; (S)-(-)-2-(tert-Butoxycarbonylamino)-1-propanol; tert-butyl N-[(1S)-2-hydroxy-1-methyl-ethyl]carbamate; N-tert-Butoxycarbonyl-L-alaninol; Carbamic acid, [(1S)-2-hydroxy-1-methylethyl]-, 1,1-dimethylethyl ester; (S)-tert-butyl 1-hydroxypropan-2-ylcarbamate; tert-Butyl [(2S)-1-hydroxypropan-2-yl]carbamate; Carbamic acid, (2-hydroxy-1-methylethyl)-, 1,1-dimethylethyl ester, (s)-; tert-butyl ((2S)-1-hydroxypropan-2-yl)carbamate; Boc-Ala-ol; boc-(s)-alaninol; (2S)-2-Aminopropan-1-ol, N-BOC protected; N-((1S)-2-hydroxy-isopropyl)(tert-butoxy)carboxamide; tert-butyl (S)-(1-hydroxypropan-2-yl)carbamate; 57BU9FA6VG; SCHEMBL57872; n-t-butoxycarbonyl-l-alaninol; orb2940346; DTXSID40427479; N-Boc-L-alaninol, Boc-L-alaninol; FD1019; AKOS015838059; N-(tert.-butyloxycarbonyl)-L-alaninol; CS-W007729; HY-W007729; (S)-2-t-butoxycarbonylamino-1-propanol; AC-23791; AS-14668; BP-12774; SY017384; DB-022715; ST50825073; (5)-tert-butyl 1-hydroxypropan-2-ylcarbamate; (S)-2-(tert-butoxycarbonyl)amino-1-propanol; (S)-tert-butyl-1-hydroxypropan-2-ylcarbamate; tert-Butyl 2-hydroxy-1-methylethylcarbamate #; (S)-tert-butyl 1 -hydroxypropan-2-ylcarbamate; EN300-156990; t-Butyl (1S)-2-hydroxy-1-methylethylcarbamate; (S)-2-(N-tert-butoxycarbonylamino)-1-propanol; t-butyl (S)-(2-hydroxy-1-methylethyl)carbamate; tert-butyl[(2S)-1-hydroxypropan-2-yl]carbamate; (S)-tert-butyl (1-hydroxypropan-2-yl)-carbamate; (S)-(?)-2-(tert-Butoxycarbonylamino)-1-propanol; tert-butyl [(1S)-2-hydroxy-1-methylethyl]carbamate; tert-Butyl[(1S)-2-hydroxy-1-methylethyl]carbamate; (S)-2-[N-(2-methyl-2-propyloxycarbonyl) amino]propanol; ((s)-2-hydroxy-1-methyl-ethyl)-carbamic acid tert-butyl ester; ((S)-2-hydroxy-1-methylethyl)carbamic acid tert-butyl ester; (1S)-2-hydroxy-1-methyl-ethyl-carbamic acid tert-butyl ester; (S)-(2-Hydroxy-1-methyl-ethyl)-carbamic acid tert-butyl ester; (S)-2-(Boc-amino)-1-propanol, 98%, optical purity ee: 98% (GLC); Carbamic acid, N-[(1S)-2-hydroxy-1-methylethyl]-, 1,1-dimethylethyl ester",175.230,C8H17NO3,

Product application:N-Boc-L-Alaninol, Boc-L-alaninol, (S)-2-(Boc-amino)-1-propanol, (S)-(-)-2-(tert-Butoxycarbonylamino)-1-propanol, N-(tert-Butoxycarbonyl)-L-alaninol, CAS 79069-13-9, 79069-13-9, Suzhou Health Chemicals Co. Ltd., Chiral pharmaceutical intermediates, Peptide synthesis building blocks, Amino alcohol derivatives, Boc protected L-alaninol, High purity N-Boc-L-Alaninol, C8H17NO3, Molecular weight 175.23, Asymmetric synthesis precursor, API intermediate supplier, N-Boc-L-Alaninol manufacturer China, Buy N-Boc-L-Alaninol CAS 79069-13-9, N-Boc-L-Alaninol factory price

 

N-Boc-L-Alaninol is a vital chiral building block and key pharmaceutical intermediate widely utilized in organic synthesis and peptide chemistry. In the pharmaceutical industry, it serves as an essential precursor for manufacturing active pharmaceutical ingredients (APIs), including antiviral agents, anti-cancer drugs, central nervous system therapeutics, and highly selective enzyme/protease inhibitors; in peptide and peptidomimetic synthesis, its Boc-protected amino structure ensures regional selectivity while building intricate bioactive peptides; in asymmetric synthesis and catalysis, it is extensively employed to construct chiral ligands, oxazoline catalysts, and chiral auxiliaries for inducing high stereoselectivity; additionally, in fine chemical and agrochemical research, N-Boc-L-Alaninol acts as a key chiral source for synthesizing next-generation, high-efficiency, eco-friendly chiral pesticides and fungicides.