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Merck

96092

Sigma-Aldrich

N-Z-1,3-丙二胺 盐酸盐

≥98.0% (AT)

别名:

N-Z-1,3-二氨基丙烷 盐酸盐, N-(3-氨丙基)氨基甲酸苄酯 盐酸盐

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About This Item

线性分子式:
C6H5CH2OCONH(CH2)3NH2 · HCl
CAS号:
分子量:
244.72
Beilstein:
4725495
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:

化驗

≥98.0% (AT)

形狀

crystals

反應適用性

reagent type: cross-linking reagent

mp

185-189 °C

官能基

Cbz
amine

SMILES 字串

[H]Cl.NCCCNC(OCC1=CC=CC=C1)=O

InChI

1S/C11H16N2O2.ClH/c12-7-4-8-13-11(14)15-9-10-5-2-1-3-6-10;/h1-3,5-6H,4,7-9,12H2,(H,13,14);1H

InChI 密鑰

XKMBTMXQMDLSRB-UHFFFAOYSA-N

其他說明

结构单元[1][2]

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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S A Boyd et al.
Journal of medicinal chemistry, 37(19), 2991-3007 (1994-09-16)
The aim of this study was the discovery of nonpeptide renin inhibitors with much improved oral absorption, bioavailability, and efficacy, for use as antihypertensive agents. Our prior efforts led to the identification of A-74273 [1,R = 3-(4-morpholino)propyl], with a bioavailability
F R Pfeiffer et al.
Journal of medicinal chemistry, 27(3), 325-341 (1984-03-01)
Tri- and tetrapeptide analogues were synthesized and evaluated as renal vasodilators. These peptides were prepared by standard coupling reactions, which also provided good yields with hindered alpha-methyl amino acid derivatives. Preliminary evidence of renal vasodilator activity was determined in anesthetized

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