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Merck
CN

96092

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
PubChem Substance ID:
57653744
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
4725495
MDL number:
MFCD00270153

Key Documents

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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

assay

≥98.0% (AT)

form

crystals

reaction suitability

reagent type: cross-linking reagent

mp

185-189 °C

functional group

Cbz, amine

Other Notes

Building block

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBR0325V
BCBJ8459V
1390123V
1390123
1381088

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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
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

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