N1-Benzyloxycarbonyl-1,3-diaminopropane hydrochloride
Names
[ CAS No. ]:
17400-34-9
[ Name ]:
N1-Benzyloxycarbonyl-1,3-diaminopropane hydrochloride
[Synonym ]:
N-Benzyloxycarbonyl-1,3-propanediamine hydrochloride
Benzyl N-(3-Aminopropyl)carbamate Hydrochloride
N-Cbz-1,3-diaminopropane Hydrochloride
Carbamic acid, N-(3-aminopropyl)-, phenylmethyl ester, hydrochloride (1:1)
Benzyl (3-aminopropyl)carbamate hydrochloride (1:1)
N-Z-1,3-Propanediamine hydrochloride
N-(3-Aminopropyl)carbamic Acid Benzyl Ester Hydrochloride
Benzyl (3-aminopropyl)carbamate hydrochloride
benzyl N-(3-aminopropyl)carbamate,hydrochloride
N-Carbobenzoxy-1,3-diaminopropane Hydrochloride
MFCD00270153
Chemical & Physical Properties
[ Density]:
1.109g/cm3
[ Boiling Point ]:
368.2ºC at 760mmHg
[ Melting Point ]:
185-189 °C
[ Molecular Formula ]:
C11H17ClN2O2
[ Molecular Weight ]:
244.718
[ Flash Point ]:
176.5ºC
[ Exact Mass ]:
244.097855
[ PSA ]:
64.35000
[ LogP ]:
3.15480
[ Vapour Pressure ]:
1.11E-06mmHg at 25°C
[ Storage condition ]:
2-8°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2924299090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2924299090
[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
J. Med. Chem. 37 , 2991, (1994)
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 t...
Tri- and tetrapeptide analogues of kinins as potential renal vasodilators.J. Med. Chem. 27 , 325, (1984)
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-m...