CAS 57260-73-8

N-BOC-etilenodiamina

Descrição:

N-BOC-etilenodiamina, também conhecido como N-tert-butiloxicarbonila-etilenodiamina, é um composto orgânico caracterizado pela presença de um grupo protetor de tert-butiloxicarbonila (BOC) ligado à estrutura de etilenodiamina. Este composto geralmente aparece como um líquido ou sólido incolor a amarelo pálido, dependendo de sua forma e pureza. É solúvel em solventes orgânicos polares, como metanol e dimetilsulfóxido, mas menos solúvel em solventes não polares. N-BOC-etilenodiamina é utilizado principalmente na síntese orgânica, particularmente na preparação de vários fármacos e agroquímicos, onde atua como um intermediário versátil. O grupo BOC fornece proteção para as funcionalidades aminas durante reações químicas, permitindo modificações seletivas. Após a desproteção, os grupos amina originais podem ser utilizados para reações adicionais. As considerações de segurança incluem manuseá-lo em uma área bem ventilada e usar o equipamento de proteção pessoal adequado, pois pode causar irritação na pele e nos olhos.

Fórmula: C₇H₁₆N₂O₂

InChI: InChI=1/C7H16N2O2/c1-7(2,3)11-6(10)9-5-4-8/h4-5,8H2,1-3H3,(H,9,10)

Chave InChI: InChIKey=AOCSUUGBCMTKJH-UHFFFAOYSA-N

SMILES: O(C(NCCN)=O)C(C)(C)C

Sinónimos:

• (2-Aminoethyl)carbamic acid 1,1-dimethylethyl ester
• (2-Aminoethyl)carbamic acid tert-butyl ester
• 1,1-Dimethylethyl (2-aminoethyl)carbamate
• 1-[(tert-Butoxycarbonyl)amino]-2-aminoethane
• 2-(N-tert-Butoxycarbonylamino)ethylamine
• 2-(tert-Butoxycarbonyl)amino-1-aminoethane
• 2-[(tert-Butoxycarbonyl)amino]ethylamine
• 2-[[(tert-Butyloxy)carbonyl]amino]ethylamine
• Carbamic acid, (2-aminoethyl)-, 1,1-dimethylethyl ester
• Carbamic acid, N-(2-aminoethyl)-, 1,1-dimethylethyl ester
• N-(2-Aminoethyl)carbamic acid 1,1-dimethylethyl ester
• N-(2-Aminoethyl)carbamic acid tert-butyl ester
• N-(t-Butyloxycarbonyl)ethylenediamine
• N-(tert-Butoxycarbonyl)-1,2-diaminoethane
• N-(tert-Butoxycarbonyl)-1,2-ethanediamine
• N-(tert-Butoxycarbonyl)ethylenediamine
• N-BOC-1,2-Diaminoethane
• N-Boc-1,2-ethylendiamine
• N-Boc-Ethane-1,2-Diamine
• N-Tert-Boc-Ethylenediamine
• N-tert-Butoxycarbonyl-1,2-ethylenediamine
• Tert-Butyl (2-Aminoethyl)Carbamate
• Tert-Butyl 2-Aminoethylcarbamate
• [(tert-Butyloxy)carbonyl]-1,2-ethylenediamine
• mono-BOC-ethylenediamine
• tert-Butyl N-(2-aminoethyl)carbamate
• tert-Butyl [(2-aminoethyl)amino]formate
• N-(2-AMINOETHYL)-N-BOC-AMINE
• N-1-T-BUTOXYCARBONYL-1,2-DIAMINOETHANE
• BUTTPARK 27\08-29
• 1-BOC-AMINO-1,2-ETHANEDIAMINE
• N-BOC-DIAMINOETHANE
• BOC-EDA
• BOC-NH-(CH2)2-NH2
• 1-BOC-ETHYLENEDIAMINE
• (2-AMINO-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER
• N-BOC-ETHYLENEDIAMINE
• N-(T-BOC)ETHYLENEDIAMINE
• AKOS 91563
• BOC-DIAMINOETHANE

N-(tert-Butoxycarbonyl)-1,2-diaminoethane

CAS: 57260-73-8

Fórmula: C₇H₁₆N₂O₂

Pureza: >97.0%(GC)

Cor e Forma: Colorless to Light yellow clear liquid

Peso molecular: 160.22

Ref: 3B-A1371

N-Boc-ethylenediamine, 98%, may cont up to 5% tert-butanol

CAS: 57260-73-8

N-Boc-ethylenediamine is used in the synthesis of thyronamine derivatives. It is also used in the preparation of (2-isothiocyanato-ethyl)-carbamic acid tert-butyl ester by reacting with carbon disulfide. Further, it is used in both oligonucleotide and peptide synthesis. This Thermo Scientific Chemic

Fórmula: C₇H₁₆N₂O₂

Pureza: 98%

Cor e Forma: Clear, colorless to pale yellow, Liquid

Peso molecular: 160.22

Ref: 02-L19947

1-Boc-ethylenediamine

CAS: 57260-73-8

Fórmula: C₇H₁₆N₂O₂

Pureza: 96%

Cor e Forma: Liquid

Peso molecular: 160.2141

Ref: IN-DA0035CX

NH2-C2-NH-Boc

CAS: 57260-73-8

NH2-C2-NH-Boc

Pureza: ≥98%

Peso molecular: 160.21g/mol

Ref: 54-BUP17428

Ethane-1,2-diamine, N-BOC protected

CAS: 57260-73-8

Ethane-1,2-diamine, N-BOC protected

Fórmula: C₇H₁₆N₂O₂

Pureza: 97%

Cor e Forma: clear. almost colourless liquid

Peso molecular: 160.21413g/mol

Ref: 54-OR1533

tert-Butyl N-(2-aminoethyl)carbamate

CAS: 57260-73-8

Fórmula: C₇H₁₆N₂O₂

Pureza: 98.0%

Cor e Forma: Liquid, Clear or Viscous

Peso molecular: 160.217

Ref: 10-F017322

NH2-C2-NH-Boc

CAS: 57260-73-8

NH2-C2-NH-Boc (PROTAC Linker 22) (PROTAC Linker 22) is a alkyl chain-based PROTAC linker. NH2-C2-NH-Boc can be used in the synthesis of PROTACs.

Fórmula: C₇H₁₆N₂O₂

Pureza: ≥98%

Cor e Forma: Colorless To Light Yellow

Peso molecular: 160.21

Ref: TM-T18616

N-Boc-ethylenediamine

CAS: 57260-73-8

Fórmula: C₇H₁₆N₂O₂

Peso molecular: 160.22

Ref: ST-EA-CP-C22042

N-Boc-ethylenediamine

CAS: 57260-73-8

N-Boc-ethylenediamine is a chemical compound that belongs to the group of peptide hormones. It is historically used as a building block for peptides, such as luteinizing hormone releasing hormone (LHRH), which control reproduction and regulate the release of hormones. N-Boc-ethylenediamine has been shown to inhibit dpp-iv, an enzyme that breaks down proteins needed for cell growth and survival. This inhibition leads to cell death by apoptosis, or programmed cell death. N-Boc-ethylenediamine has also been shown to be an antimicrobial peptide against gram negative bacteria. The synthesis of this compound can be accomplished through several methods, including using diazonium salt or histone proteins. The analytical method involves hydrogen bonding between the amines and trifluoroacetic acid in order to produce the desired product.

Fórmula: C₇H₁₆N₂O₂

Pureza: Min. 95%

Cor e Forma: Clear Liquid

Peso molecular: 160.21 g/mol

Ref: 3D-FB18943

NH2-C2-NH-Boc

Produto Controlado

CAS: 57260-73-8

Applications N-Boc-ethylenediamine is used in the synthesis of Thyronamine derivatives and analogs.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Anon., et al.: J. Pharmacol., 58, 53 (1936), Boissier, J., et al.: Eur. J. Pharmacol., 22, 141 (1973), Nillne, E., et al.: J. Biol. Chem., 277, 48587 (2002),

Fórmula: C₇H₁₆N₂O₂

Cor e Forma: Neat

Peso molecular: 160.21

Ref: TR-B655000

NHS-dPEG®4-Biotinidase Resistant Biotin

CAS: 57260-73-8

NHS-dPEG®4-Biotinidase Resistant Biotin is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. NHS-dPEG®4-Biotinidase Resistant Biotin is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.

Fórmula: C₁₅H₃₂N₂O₅

Pureza: Min. 95%

Peso molecular: 160.21 g/mol

Ref: 3D-DPG-6277

tert-butyl (2-aminoethyl)carbamate

CAS: 57260-73-8

Fórmula: C₇H₁₆N₂O₂

Peso molecular: 160.21

Ref: ST-EA-CP-S43032