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15404

Sigma-Aldrich

N-Boc-1,4-butanediamine

≥97.0% (GC/NT)

Sinonimo/i:

N-Boc-1,4-diaminobutane, tert-Butyl N-(4-aminobutyl)carbamate

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About This Item

Formula condensata:
(CH3)3COCONH(CH2)4NH2
Numero CAS:
68076-36-8
Peso molecolare:
188.27
Beilstein:
1937878
Numero MDL:
MFCD00210019
Codice UNSPSC:
12352116
ID PubChem:
57647412
NACRES:
NA.22

Livello qualitativo

100

Saggio

≥97.0% (GC/NT)

Impiego in reazioni chimiche

reagent type: cross-linking reagent

Indice di rifrazione

n20/D 1.460

Densità

0.984 g/mL at 20 °C (lit.)

Gruppo funzionale

Boc
amine

Stringa SMILE

NCCCCNC(OC(C)(C)C)=O

InChI

1S/C9H20N2O2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7,10H2,1-3H3,(H,11,12)
ZFQWJXFJJZUVPI-UHFFFAOYSA-N

Categorie correlate

Applicazioni

  • Carboxy-Silane Coated Iron Oxide Nanoparticles: Details the application of N-Boc-1,4-butanediamine in modifying iron oxide nanoparticles for imaging and drug delivery (D Stanicki, S Boutry, S Laurent, et al., 2014). Access the article.

Altre note

Preparation of pharmacologically active compounds. Preparation of spermidine analogues. Introduction of a C4-spacer.

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314

Classi di pericolo

Skin Corr. 1B

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

228.2 °F - closed cup

Punto d’infiammabilità (°C)

109.0 °C - closed cup

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
1142779V
1142779
015906/2
062192/1
015906/1

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N-Boc-4,7,10-trioxa-1,13-tridecanediamine ≥95.0% (NT)

Sigma-Aldrich

93113

N-Boc-4,7,10-trioxa-1,13-tridecanediamine

Y Shai et al.
Biochemistry, 28(11), 4801-4806 (1989-05-30)
In the present study we synthesize 18F-labeled insulin of high specific radioactivity. A new prosthetic group methodology, in which [18F]fluoride displaces a bromide group of 4-(bromomethyl)-benzoylamine intermediates, was used. The 4-(fluoromethyl)benzoyl product was chemically stable. 18F-Labeled insulin retains the essential
L I Kruse et al.
Journal of medicinal chemistry, 32(2), 409-417 (1989-02-01)
In an attempt to identify a soluble oncodazole analogue that could be easily formulated, a series of substituted oncodazoles was synthesized and evaluated for tubulin binding affinity, in vitro cytotoxicity against cultured mouse B-16 cells, and ability to prolong lifespan
Hongyan Guo et al.
Journal of medicinal chemistry, 45(10), 2056-2063 (2002-05-03)
Several iron chelators containing alpha,beta-unsaturated hydroxamic acid motifs appended to a citric acid platform were synthesized. Mycobacterium paratuberculosis was then challenged to grow in the presence of a panel of siderophores (mycobactin J, deferrioxamine B, acinetoferrin, and nannochelin A) and
M. McWatt, G.J. Boons et al.
European Journal of Organic Chemistry, 2535-2535 (2001)
H.H. Wassermann et al
Tetrahedron, 58, 7177-7177 (2002)
Visualizza tutti i documenti correlati

Articoli

MRT - Mono-Boc-Protection of Diamines

Mono-Boc-protected diamines are versatile building blocks for chemical synthesis. Their production is a lot more challenging than the simple reaction scheme might imply, because the Boc-anhydride reagent cannot differentiate between the two identical amino moieties in the substrate.

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

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