CAS 47355-10-2

N(alpha)-boc-N(in)-formyl-L-tryptophan

Description:

N(alpha)-Boc-N(in)-formyl-L-tryptophan is a derivative of the amino acid tryptophan, characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group at the alpha-amino group and a formyl group at the indole nitrogen. This compound is typically used in peptide synthesis and as an intermediate in the preparation of more complex molecules. The Boc group serves to protect the amino group during chemical reactions, allowing for selective modifications of other functional groups. The formyl group introduces a reactive aldehyde functionality, which can participate in various chemical reactions, including condensation and cyclization. This compound is generally stable under standard laboratory conditions but may be sensitive to moisture and heat. Its solubility is typically in organic solvents, making it suitable for use in organic synthesis. As with many amino acid derivatives, it may exhibit biological activity, and its derivatives can be explored for potential pharmaceutical applications. Proper handling and storage conditions are essential to maintain its integrity and reactivity.

Formula: C₁₇H₂₀N₂O₅

InChI: InChI=1/C17H20N2O5/c1-17(2,3)24-16(23)18-13(15(21)22)8-11-9-19(10-20)14-7-5-4-6-12(11)14/h4-7,9-10,13H,8H2,1-3H3,(H,18,23)(H,21,22)/t13-/m0/s1

SMILES: CC(C)(C)OC(=N[C@@H](Cc1cn(C=O)c2ccccc12)C(=O)O)O

Synonyms:

• na-T-boc-N-in-formyl-L-tryptophan
• Boc-Trp(For)-OH
• Boc-Trp(CHO)-OH
• N-alpha-t-butyloxycabonyl-N-formyl-L-tryptophane
• N alpha-(tert-Butoxycarbonyl)-N1-formyl-L-tryptophan
• N-(tert-butoxycarbonyl)-1-formyl-L-tryptophan
• N-α-Boc-N-in-formyl-L-tryptophan
• (Tert-Butoxy)Carbonyl Trp(For)-OH
• N-ALPHA-T-BOC-N-FORMYL-L-TRYPTOPHAN
• BOC-TRP(FOR)-OH USP/EP/BP
• NALPHA-(TERT-BUTOXYCARBONYL)-N1-FORMYL-L-TRYPTOPHAN
• Nα-Boc-Nin-formyl-L-tryptophan
• (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(1-formyl-1H-indol-3-yl)propanoic acid
• N-Boc-1-forMyl-L-tryptophan, 98%
• N-ALPHA-T-BOC-N-IN-FORMYL-L-TRYPTOPHAN
• Boc-L-Trp(Formyl)-OH.solvent
• BOC-NIN-FORMYL-L-TRYPTOPHAN
• Nalpha-(tert-butoxycarbonyl)-N-in-formyl-L-tryptophan
• N-tert-Butoxycarbonyl-N-formyl-L-tryptophan
• Nalpha-Boc-N1-formyl-L-tryptophan
• Nα-(tert-Butoxycarbonyl)-N1-formyl-L-tryptophan
• N
• BOC-L-TRYPTOPHAN(NIN-FORMYL)
• L-Tryptophan, N-[(1,1-dimethylethoxy)carbonyl]-1-formyl-
• N-ALPHA-T-BUTYLOXYCARBONYL-N''-FORMYL-L-TRYPTOPHANE
• Nα-Boc-Nin-formyl-L-tryptophan99%
• N-a-(tert-Butoxycarbonyl)-N1-formyl-L-tryptophan
• α
• N-ALPHA-TERT-BUTYLOXYCABONYL-N'-FORMYL-L-TRYPTOPHANE
• BOC-L-TRP(FORMYL)-OH
• BOC-TRYPTOPHAN(FOR)-OH
• (S)-2-((tert-Butoxycarbonyl)aMino)-3-(1-forMyl-1H-indol-3-yl)propanoic acid
• (2S)-3-(1-formylindol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoicaci
• N-ALPHA-TERT-BUTYLOXYCARBONYL-N'-FORMYL-L-TRYPTOPHANE
• BOC-TRP(CHO)
• NALPHA-tert-Butoxycarbonyl-Nin-formyl-L-tryptophane
• NALPHA-BOC-N1-FORMYL-L-TRYPTOPHAN
• N-ALPHA-T-BUTYLOXYCARBONYL-NIN-FORMYL-L-TRYPTOPHAN
• N-ALPHA-T-BUTOXYCARBONYL-N-INDOLE-FORMYL-L-TRYPTOPHAN
• N-tert-Butoxycarbonyl-N(in)-formyl-L-tryptophan
• 3-(1-formyl-3-indolyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid
• BOC-(FORMYL)-TRYPTOPHAN
• BOC-L-TRP(FOR)-OH
• -Boc-N(in)-formyl-L-tryptophan
• Nα-(tert-Butoxycarbonyl)-N1-formyl-L-tryptophan &gt
• N-ALPHA-TERT-BUTYLOXYCARBONYL-N'-FORMYL-L-TRYPTOPHAN
• -Boc-N-Formyl-L-tryptophan, 98%
• NALPHA-BOC-N(IN)-FORMYL-L-TRYPTOPHAN
• (2S)-2-(tert-Butoxycarbonylamino)-3-(1-formylindol-3-yl)propanoic acid

Boc-Trp(For)-OH

CAS: 47355-10-2

Standard Trp derivative in Boc-SPPS. Odagami et al. achieved deformylation in excellent yield employing N,N’-dimethylethylenediamine in water.

Formula: C₁₇H₂₀N₂O₅

Purity: 98.6%

Color and Shape: Whitish

Molecular weight: 332.36

Ref: 01-4001264

Boc-Trp(For)-OH

CAS: 47355-10-2

Formula: C₁₇H₂₀N₂O₅

Purity: 95%

Color and Shape: Solid

Molecular weight: 332.3511

Ref: IN-DA003OHJ

Boc-Trp(For)-OH

CAS: 47355-10-2

Molecular weight: 332.35

Ref: 7W-GM1040

(2S)-2-(tert-Butoxycarbonylamino)-3-(1-formylindol-3-yl)propanoic acid

CAS: 47355-10-2

(2S)-2-(tert-Butoxycarbonylamino)-3-(1-formylindol-3-yl)propanoic acid

Formula: C₁₇H₂₀N₂O₅

Purity: 95%

Molecular weight: 332.35109

Ref: 54-OR480669

Boc-Trp(CHO)-OH

CAS: 47355-10-2

Boc-Trp(CHO)-OH is a peptide that is an activator of the ion channel TRPV1. It binds to the receptor for capsaicin and then causes a conformational change in the receptor protein, which leads to activation of the ion channel. Boc-Trp(CHO)-OH is used as a research tool in pharmacology, cell biology, and antibody production. This peptide can be synthesized with high purity and has been shown to have inhibitory effects on TRPV1 channels.

Formula: C₁₇H₂₀N₂O₅

Purity: Min. 95%

Molecular weight: 332.35 g/mol

Ref: 3D-BLW-2115

Boc-Trp(For)-OH

CAS: 47355-10-2

M03329 - Boc-Trp(For)-OH

Formula: C₁₇H₂₀N₂O₅

Purity: 95%

Color and Shape: Solid, Beige powder

Molecular weight: 332.356

Ref: 10-M03329