![O-(1,1-Dimethylethyl)-N-[(phenylmethoxy)carbonyl]-L-threonine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F15408-o-11-dimethylethyl-n-phenylmethoxy-carbonyl-l-threonine.webp&w=3840&q=75)
CAS 16966-09-9: O-(1,1-Dimethylethyl)-N-[(phenylmethoxy)carbonyl]-L-threonine
Formula:C16H23NO5
InChI:InChI=1S/C16H23NO5/c1-11(22-16(2,3)4)13(14(18)19)17-15(20)21-10-12-8-6-5-7-9-12/h5-9,11,13H,10H2,1-4H3,(H,17,20)(H,18,19)/t11-,13+/m1/s1
InChI key:InChIKey=QJYMOTAFFJDTAG-YPMHNXCESA-N
SMILES:[C@H](NC(OCC1=CC=CC=C1)=O)([C@H](OC(C)(C)C)C)C(O)=O
Synonyms:- <span class="text-smallcaps">L</span>-Threonine, O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-
- Butyric acid, 3-tert-butoxy-2-(carboxyamino)-, N-benzyl ester
- N-(Benzyloxycarbonyl)-O-tert-butyl-<span class="text-smallcaps">L</span>-threonine
- N-[(Benzyloxy)carbonyl]-O-tert-butyl-L-threonine
- O-(1,1-Dimethylethyl)-N-[(phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-threonine
- L-Threonine, O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-
- O-(1,1-Dimethylethyl)-N-[(phenylmethoxy)carbonyl]-L-threonine
- N-(Benzyloxycarbonyl)-O-tert-butyl-L-threonine
Sort by
Found 4 products.
(2S,3R)-2-(((Benzyloxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:309.36199951171875L-Threonine, O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-
CAS:Formula:C16H23NO5Purity:97%Color and Shape:SolidMolecular weight:309.3575N-((Benzyloxy)Carbonyl)-O-(Tert-Butyl)-L-Threonine
CAS:N-((Benzyloxy)Carbonyl)-O-(Tert-Butyl)-L-ThreoninePurity:98%+Molecular weight:309.36g/mol(2S,3R)-2-(((Benzyloxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid
CAS:(2S,3R)-2-(((Benzyloxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid, also known as (2S,3R)-2-(((benzyloxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid or 2S,3R-Dibenzylglycine tert-Butyl Ester is an amino acid that is used in the synthesis of peptides. It is a biochemical that can be synthesized from l-threonine and chloroformate. This compound can be derived from plant sources such as saponified castor oil. The synthesis of this compound involves the dehydration of isobutene to form tetrahydrofuran and then reacting it with thionyl chloride to produce chloride ions. The l-threonine methyl ester reacts with the chloride ion to form an activated esterFormula:C16H23NO5Purity:Min. 95%Molecular weight:309.36 g/mol
![L-Threonine, O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA0037OZ.jpg&w=3840&q=75)
