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Merck
CN

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编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

方案

≥98.0% (AT)

表单

crystals

反应适用性

reagent type: cross-linking reagent

mp

185-189 °C

官能团

Cbz
amine

SMILES字符串

[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 key

XKMBTMXQMDLSRB-UHFFFAOYSA-N

其他说明

结构单元

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

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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