CAS 7536-58-5

N-terc-butiloxicarbonil-L-ácido aspártico β-éster benzílico

Descrição:

N-terc-butiloxicarbonil-L-ácido aspártico β-éster benzílico, comumente referido como Boc-L-Asp(β-Bn) ou pelo seu número CAS 7536-58-5, é um derivado de aminoácido usado principalmente na síntese de peptídeos e na química orgânica. Este composto apresenta um grupo protetor de tert-butiloxicarbonilo (Boc), que é comumente empregado para proteger o grupo amino durante a síntese de peptídeos, permitindo reações seletivas em outros grupos funcionais. O moiety de éster β-benzila melhora a lipofilicidade da molécula, facilitando sua incorporação em várias reações orgânicas. N-terc-butiloxicarbonil-L-ácido aspártico β-éster benzílico é tipicamente um sólido branco a off-white e é solúvel em solventes orgânicos como diclorometano e metanol, mas menos solúvel em água. Sua estrutura inclui um grupo funcional ácido carboxílico, que pode participar de transformações químicas adicionais. O composto é valioso na síntese de peptídeos e outras moléculas bioativas, tornando-o significativo na pesquisa farmacêutica e bioquímica. O manuseio e armazenamento adequados são essenciais devido à sua reatividade potencial e à necessidade de condições específicas durante a síntese.

Fórmula: 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

Chave InChI: InChIKey=SOHLZANWVLCPHK-LBPRGKRZSA-N

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

Sinónimos:

• (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

Fórmula: C₁₆H₂₁NO₆

Pureza: >98.0%(T)

Cor e Forma: White to Almost white powder to crystal

Peso molecular: 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

Fórmula: C₁₆H₂₁NO₆

Pureza: 98%

Cor e Forma: White, Powder

Peso molecular: 323.35

Ref: 02-B21758

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

Bachem ID: 4000620.

Fórmula: C₁₆H₂₁NO₆

Pureza: 98.1%

Cor e Forma: White

Peso molecular: 323.35

Ref: 01-4000620

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

Fórmula: C₁₆H₂₁NO₆

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 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.

Fórmula: C₁₆H₂₁NO₆

Pureza: 99.57%

Cor e Forma: Solid

Peso molecular: 323.34

Ref: TM-T64335

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

Fórmula: C₁₆H₂₁NO₆

Peso molecular: 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

Fórmula: C₁₆H₂₁NO₆

Pureza: 98%

Cor e Forma: white solid

Peso molecular: 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)

Pureza: ≥98%

Peso molecular: 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.

Fórmula: C₁₆H₂₁NO₆

Pureza: Min. 95%

Peso molecular: 323.34 g/mol

Ref: 3D-BLD-2059

Boc-Asp(OBzl)-OH

CAS: 7536-58-5

M03266 - Boc-Asp(OBzl)-OH

Fórmula: C₁₆H₂₁NO₆

Pureza: 98%

Cor e Forma: Solid, Crystalline Powder

Peso molecular: 323.345

Ref: 10-M03266

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

CAS: 7536-58-5

Fórmula: C₁₆H₂₁NO₆

Pureza: min. 98%

Cor e Forma: White to off-white, Crystalline powder

Peso molecular: 323.34

Ref: SR-12202