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Documenti fondamentali

15408

Sigma-Aldrich

N-Boc-1,3-propanediamine

≥97.0% (GC/NT)

Sinonimo/i:

N-Boc-1,3-diaminopropane, tert-Butyl N-(3-aminopropyl)carbamate

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About This Item

Formula condensata:
(CH3)3COCONH(CH2)3NH2
Numero CAS:
Peso molecolare:
174.24
Beilstein:
3588328
Numero MDL:
Codice UNSPSC:
12352116
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Saggio

≥97.0% (GC/NT)

Impiego in reazioni chimiche

reagent type: cross-linking reagent

Indice di rifrazione

n20/D 1.454 (lit.)
n20/D 1.459

P. ebollizione

203 °C (lit.)

Punto di fusione

22 °C (lit.)

Densità

0.998 g/mL at 20 °C (lit.)

Gruppo funzionale

Boc
amine

Stringa SMILE

NCCCNC(OC(C)(C)C)=O

InChI

1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6,9H2,1-3H3,(H,10,11)
POHWAQLZBIMPRN-UHFFFAOYSA-N

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Applicazioni

  • Tackling vancomycin-resistant bacteria with ′lipophilic–vancomycin–carbohydrate conjugates′: This study discusses the synthesis of derivatives using N-Boc-1,3-propanediamine to develop new antibacterial agents targeting resistant bacterial strains (Yarlagadda et al., 2015).
  • Sulfonamides differing in the alkylamino substituent length–Synthesis, electrochemical characteristic, acid-base profile and complexation properties: The study involves N-Boc-1,3-propanediamine in the synthesis of novel sulfonamide derivatives with potential biochemical applications (Ciesielska et al., 2022).
  • Direct α-alkylation of primary aliphatic amines enabled by CO2 and electrostatics: Research demonstrating selective α-alkylation of N-Boc-1,3-propanediamine, highlighting a novel method in organic synthesis (Ye et al., 2018).

Altre note

Synthesis of spermidine analogues; Preparation of pharmacologically active compounds.

Pittogrammi

CorrosionExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - 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 °C - closed cup

Dispositivi di protezione individuale

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


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B. Plouvier et al.
Heterocycles, 32, 693-693 (1991)
T L Huang et al.
Journal of medicinal chemistry, 35(13), 2414-2418 (1992-06-26)
A number of substrate analogues of N8-acetylspermidine (N8-AcSpd) (16) and chemical modifying agents containing metal coordinating ligands were assayed as inhibitors of the cytoplasmic enzyme N8-AcSpd deacetylase from rat liver. The enzyme is inhibited by metal chelators, several omega-amino-substituted carboxylic
Syota Kawaguchi et al.
The Journal of reproduction and development, 59(3), 219-224 (2013-02-07)
Luteoprotective mechanisms of luteinizing hormone (LH) involved in the maintenance of bovine corpus luteum (CL) function have not been completely clarified. Since antioxidant enzymes are well documented as antiapoptotic factors in the CL of many mammals, we hypothesized that the
Syota Kawaguchi et al.
The Journal of reproduction and development, 59(3), 225-230 (2013-01-30)
Luteinizing hormone (LH) regulates several ovarian functions. However, the luteoprotective mechanisms of LH involved in the maintenance of bovine corpus luteum (CL) function are not well understood. Since prostaglandin F2α (PGF), PGE2 and progesterone (P4) are well documented as antiapoptotic
Yuki Yamamoto et al.
Reproduction, fertility, and development, 28(6), 673-681 (2014-11-06)
Endothelin (EDN) is a possible regulating factor of oviductal motility, which is important for the transport of gametes and embryo. To clarify the factors that control the secretion of EDN in the bovine oviduct, the expression of EDNs, EDN-converting enzymes

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