CAS 157355-81-2

Fmoc-D-Thr-OH

Description:

Fmoc-D-Thr-OH, or 9-fluorenylmethoxycarbonyl-D-threonine, is a protected amino acid commonly used in peptide synthesis. It features a fluorenylmethoxycarbonyl (Fmoc) group, which serves as a protective group for the amino functionality, allowing for selective reactions during peptide assembly. The D-threonine component indicates that the amino acid is in its D-enantiomer form, which is less common than the L-form in biological systems. This compound is typically a white to off-white solid and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and methanol, but less soluble in water. The Fmoc group can be removed under basic conditions, facilitating the subsequent coupling of amino acids in peptide synthesis. Fmoc-D-Thr-OH is utilized in various applications, including the development of pharmaceuticals and in the study of protein structure and function. Its stability and ease of handling make it a valuable reagent in organic and medicinal chemistry.

Formula: C₁₉H₁₉NO₅

InChI: InChI=1/C19H19NO5/c1-11(21)17(18(22)23)20-19(24)25-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16-17,21H,10H2,1H3,(H,20,24)(H,22,23)/t11?,17-/m1/s1

SMILES: CC([C@H](C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12)O

Synonyms:

• N-Alpha-(9-Fluorenylmethoxycarbonyl)-D-Threonine
• N-Alpha-Fmoc-D-Threonine
• N-Alpha-Fmoc-D-Threonine / (2R,3S)
• Fmoc-D-Thr
• Fmoc-D-Threonine
• Fmoc-D-Thr Br
• N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-threonine
• N-Fmoc-D-Threonine
• FMOC-D-THREONINE extrapure
• N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-allothreonine
• -[(9
• (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-threonine
• D-Threonine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
• H
• FMOC-D-THR-OH USP/EP/BP
• -Fluoren-9-ylMethoxy)carbonyl]-
• N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-threonine&gt
• N
• D
• -threonine
• (2R,3S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxybutanoicaci
• (2R,3S)-3-(2-{4-[(2S)-2-carboxy-2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetamido]ethyl]phenoxy}-2-methylpropoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoic acid
• N-α-(9-Fluorenylmethoxycarbonyl)-D-threonine

D-Threonine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

CAS: 157355-81-2

Formula: C₁₉H₁₉NO₅

Purity: 97%

Color and Shape: Solid

Molecular weight: 341.3579

Ref: IN-DA001PE2

N-[(9H-Fluoren-9-Ylmethoxy)Carbonyl]-D-Threonine

CAS: 157355-81-2

N-[(9H-Fluoren-9-Ylmethoxy)Carbonyl]-D-Threonine

Purity: 98%

Molecular weight: 341.36g/mol

Ref: 54-OR1014164

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-threonine

CAS: 157355-81-2

Formula: C₁₉H₁₉NO₅

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 341.36

Ref: 3B-F0608

Fmoc-D-Threonine

CAS: 157355-81-2

Formula: C₁₉H₁₉NO₅

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 341.363

Ref: 10-F224380

FMOC-D-Threonine extrapure, 98%

CAS: 157355-81-2

Formula: C₁₉H₁₉NO₅

Purity: min. 98%

Color and Shape: White to off-white, Crystalline powder

Molecular weight: 341.40

Ref: SR-56859

(2R,3S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid

CAS: 157355-81-2

(2R,3S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid is a peptide that can be synthesized on the solid phase. It has been shown to have an adsorption mechanism that is similar to that of natural peptides. This compound has conformational and structural homology with other peptides, such as l-amino acids and threonine. The glycopeptide is a glycosylated molecule with an α-(1→6)-linked glucose at the nonterminal amino group.

Formula: C₁₉H₁₉NO₅

Purity: Min. 95%

Molecular weight: 341.4 g/mol

Ref: 3D-HGA35581