CAS 7536-58-5

N-terz-butilossicarbonil-L-acido aspartico β-estere benzilico

Descrizione:

N-terz-butilossicarbonil-L-acido aspartico β-estere benzilico, comunemente noto come Boc-L-Asp(β-Bn) o con il suo numero CAS 7536-58-5, è un derivato di aminoacido utilizzato principalmente nella sintesi di peptidi e nella chimica organica. Questo composto presenta un gruppo protettivo tert-butilossicarbonilico (Boc), comunemente impiegato per proteggere il gruppo amminico durante la sintesi di peptidi, consentendo reazioni selettive in altri gruppi funzionali. Il moiety dell'estere β-benzilico migliora la lipofilia della molecola, facilitando la sua incorporazione in varie reazioni organiche. N-terz-butilossicarbonil-L-acido aspartico β-estere benzilico è tipicamente un solido bianco a bianco sporco ed è solubile in solventi organici come il diclorometano e il metanolo, ma meno solubile in acqua. La sua struttura include un gruppo funzionale acido carbossilico, che può partecipare a ulteriori trasformazioni chimiche. Il composto è prezioso nella sintesi di peptidi e altre molecole bioattive, rendendolo significativo nella ricerca farmaceutica e biochimica. La corretta manipolazione e conservazione sono essenziali a causa della sua potenziale reattività e della necessità di condizioni specifiche durante la sintesi.

Formula: C₁₆H₂₁NO₆

InChI: InChI=1/C16H21NO6/c1-16(2,3)23-15(21)17-12(14(19)20)9-13(18)22-10-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,19,20)/t12-/m0/s1

InChI key: InChIKey=SOHLZANWVLCPHK-LBPRGKRZSA-N

SMILES: C(OC(C[C@H](NC(OC(C)(C)C)=O)C(O)=O)=O)C1=CC=CC=C1

Sinonimi:

• (2S)-2-[(2-Methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid
• (2S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid
• (2S)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoate
• (2S)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
• (S)-2-tert-Butoxycarbonylaminosuccinic acid 4-benzyl ester
• (S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid
• 4-(Benzyloxy)-2-[(Tert-Butoxycarbonyl)Amino]-4-Oxobutanoic Acid (Non-Preferred Name)
• 4-Benzylhydrogen-N-(tert-butoxycarbonyl)-L-aspartat
• 4-benzyl hydrogen N-(tert-butoxycarbonyl)-L-aspartate
• <span class="text-smallcaps">L</span>-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester
• Aspartic acid, N-carboxy-, 4-benzyl N-tert-butyl ester, <span class="text-smallcaps">L</span>-
• Aspartic acid, N-carboxy-, 4-benzyl N-tert-butyl ester, L-
• Boc-<span class="text-smallcaps">L</span>-Asp(OBn)-OH
• Boc-Asp(OBzl)-OH
• Boc-L-aspartic acid 4-benzyl ester
• Hydrogeno-N-(tert-butoxycarbonyl)-L-aspartate de 4-benzyle
• L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester
• N-(tert-Butoxycarbonyl)aspartic acid β-benzyl ester
• N-(tert-Butyloxycarbonyl)-<span class="text-smallcaps">L</span>-aspartic acid β-benzyl ester
• N-(tert-Butyloxycarbonyl)-L-aspartic acid β-benzyl ester
• N-(tert-Butyloxycarbonyl)-β-benzyl-<span class="text-smallcaps">L</span>-aspartic acid
• N-(tert-Butyloxycarbonyl)-β-benzyl-L-aspartic acid
• N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-aspartic acid 4-(phenylmethyl) ester
• N-[(1,1-Dimethylethoxy)carbonyl]-L-aspartic acid 4-(phenylmethyl) ester
• N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-aspartic acid 4-benzyl ester
• N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-aspartic acid β-benzyl ester
• N-tert-Butoxycarbonyl-L-aspartic acid 4-benzyl ester
• N-tert-Butoxycarbonyl-L-aspartic acid β-benzyl ester
• N-tert.-Butoxycarbonyl-<span class="text-smallcaps">L</span>-aspartic acid 4-phenylmethyl ester
• hidrogeno-N-(terc-butoxicarbonil)-L-aspartato de 4-bencilo
• β-Benzyl N-tert-butoxycarbonylaspartate
• BOC-ASP(OBZL)
• BOC-BETA-BENZYLESTER L-ASPARTIC ACID
• N-ALPHA-T-BOC-L-ASPARTIC-BETA-BENZYL ESTER
• BOC-ASPARTIC ACID BETA-BENZYL ESTER
• BOC-L-ASPARTIC ACID B-BENZYL ESTER
• N-ALPHA-T-BUTOXYCARBONYL-L-ASPARTIC ACID BETA-BENZYL ESTER
• BOC-L-ASP(OBZL)-OH
• N-BOC-L-ASPARTIC ACID 4-BENZYL ESTER
• BOC-L-ASPARTIC ACID (OBZL)
• BOC-ASPARTIC ACID(OBZL)-OH
• BOC-L-ASP(BZL)-OH
• N-ALPHA-TERT-BUTYLOXYCARBONYL-L-ASPARTIC ACID BETA-BENZYL ESTER
• BOC-L-ASPARTIC ACID BETA-BENZYL ESTER
• BOC-L-ASP(OBZL)
• N-ALPHA-T-BOC-L-ASPARTIC ACID BETA-BENZYL ESTER
• 4-BENZYL N-(TERT-BUTOXYCARBONYL)-L-ASPARTATE

4-Benzyl N-(tert-Butoxycarbonyl)-L-aspartate

CAS: 7536-58-5

Formula: C₁₆H₂₁NO₆

Purezza: >98.0%(T)

Colore e forma: White to Almost white powder to crystal

Peso molecolare: 323.35

Ref: 3B-B1628

N-Boc-L-aspartic acid 4-benzyl ester, 98%

CAS: 7536-58-5

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₁₆H₂₁NO₆

Purezza: 98%

Colore e forma: White, Powder

Peso molecolare: 323.35

Ref: 02-B21758

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

Bachem ID: 4000620.

Formula: C₁₆H₂₁NO₆

Purezza: 98.1%

Colore e forma: White

Peso molecolare: 323.35

Ref: 01-4000620

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

Formula: C₁₆H₂₁NO₆

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 323.3410

Ref: IN-DA0038GO

Boc-L-aspartic acid 4-benzyl ester

CAS: 7536-58-5

Boc-L-aspartic acid 4-benzyl ester (Boc-Asp(OBzl)-OH) is an aspartic acid derivative.

Formula: C₁₆H₂₁NO₆

Purezza: 99.57%

Colore e forma: Solid

Peso molecolare: 323.34

Ref: TM-T64335

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

Formula: C₁₆H₂₁NO₆

Peso molecolare: 323.35

Ref: 7W-GM3879

(2S)-2-Amino-4-(benzyloxy)-4-oxobutanoic acid, N-BOC protected

CAS: 7536-58-5

(2S)-2-Amino-4-(benzyloxy)-4-oxobutanoic acid, N-BOC protected

Formula: C₁₆H₂₁NO₆

Purezza: 98%

Colore e forma: white solid

Peso molecolare: 323.34g/mol

Ref: 54-OR46046

Boc-L-aspartic acid 4-benzyl ester, 10mM (in DMSO)

CAS: 7536-58-5

Boc-L-aspartic acid 4-benzyl ester, 10mM (in DMSO)

Purezza: ≥98%

Peso molecolare: 323.34g/mol

Ref: 54-BUP19105

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

Boc-Asp(OBzl)-OH is a cyclic peptide analog with an amino acid sequence homologous to the natural substrate of soybean trypsin. It has been shown to inhibit thrombin by intramolecular hydrogen bonding. Boc-Asp(OBzl)-OH has also been used as a prodrug for the synthesis of other analogs, such as Asp(OBzl)-Bz-NH2, which inhibits human immunodeficiency virus type 1 (HIV-1) protease. This inhibitor has been found to be effective in vitro and in vivo against HIV-1 strains that are resistant to other protease inhibitors, such as saquinavir, indinavir, and ritonavir.

Formula: C₁₆H₂₁NO₆

Purezza: Min. 95%

Peso molecolare: 323.34 g/mol

Ref: 3D-BLD-2059

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

M03266 - Boc-Asp(OBzl)-OH

Formula: C₁₆H₂₁NO₆

Purezza: 98%

Colore e forma: Solid, Crystalline Powder

Peso molecolare: 323.345

Ref: 10-M03266

BOC-L-Aspartic Acid-4-Benzylester extrapure, 98%

CAS: 7536-58-5

Formula: C₁₆H₂₁NO₆

Purezza: min. 98%

Colore e forma: White to off-white, Crystalline powder

Peso molecolare: 323.34

Ref: SR-12202