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96092

Sigma-Aldrich

N-Z-1,3-Propanediamine hydrochloride

≥98.0% (AT)

Synonym(s):

N-Z-1,3-Diaminopropane hydrochloride, Benzyl N-(3-aminopropyl)carbamate hydrochloride

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About This Item

Linear Formula:
C6H5CH2OCONH(CH2)3NH2 · HCl
CAS Number:
17400-34-9
Molecular Weight:
244.72
Beilstein:
4725495
MDL number:
MFCD00270153
UNSPSC Code:
12352200
PubChem Substance ID:
57653744

Assay

≥98.0% (AT)

form

crystals

reaction suitability

reagent type: cross-linking reagent

mp

185-189 °C

functional group

Cbz
amine

SMILES string

[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

Other Notes

Building block

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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