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Merck
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文件

15408

Sigma-Aldrich

N-叔丁氧羰基-1,3-丙二胺

≥97.0% (GC/NT)

别名:

N-(3-氨基丙基)氨基甲酸叔丁酯, N-Boc-1,3-二氨基丙烷

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About This Item

线性分子式:
(CH3)3COCONH(CH2)3NH2
CAS号:
75178-96-0
分子量:
174.24
Beilstein:
3588328
MDL號碼:
MFCD00210021
分類程式碼代碼:
12352116
PubChem物質ID:
57647415
NACRES:
NA.22

品質等級

100

化驗

≥97.0% (GC/NT)

反應適用性

reagent type: cross-linking reagent

折射率

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

bp

203 °C (lit.)

mp

22 °C (lit.)

密度

0.998 g/mL at 20 °C (lit.)

官能基

Boc
amine

SMILES 字串

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)

InChI 密鑰

POHWAQLZBIMPRN-UHFFFAOYSA-N

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相关类别

應用

  • 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).

其他說明

合成亚精胺类似物；制备药理活性化合物。

象形圖

CorrosionExclamation mark
GHS05,GHS07

訊號詞

Danger

危險聲明

H302,H314

危險分類

Acute Tox. 4 Oral - Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

228.2 °F - closed cup

閃點（°C）

109 °C - closed cup

個人防護裝備

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

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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
B. Plouvier et al.
Heterocycles, 32, 693-693 (1991)
Hironori Abe et al.
The Journal of reproduction and development, 61(4), 277-286 (2015-05-01)
We recently demonstrated that luteal cells flow out from the ovary via lymphatic vessels during luteolysis. However, the regulatory mechanisms of the outflow of luteal cells are not known. Matrix metalloproteinases (MMPs) can degrade the extracellular matrix and basal membrane
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
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
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