N-Boc-1,5-diaminopentane
Names
[ CAS No. ]:
51644-96-3
[ Name ]:
N-Boc-1,5-diaminopentane
[Synonym ]:
N-Boc-cadaverine
N-(5-Aminopentyl)carbamic Acid tert-Butyl Ester
tert-Butyl (5-aminopentyl)carbamate
N-(tert-Butoxycarbonyl)-1,5-pentanediamine
N-Boc-1,5-diaminopentane
tert-butyl N-(5-aminopentyl)carbamate
N-Boc-1,5-pentanediamine
2-Methyl-2-propanyl (5-aminopentyl)carbamate
Carbamic acid, N-(5-aminopentyl)-, 1,1-dimethylethyl ester
N-(5-Aminoamyl)carbamic Acid tert-Butyl Ester
MFCD00210020
N-(tert-Butoxycarbonyl)-1,5-diaminopentane
Biological Activity
[Description]:
[Related Catalog]:
[Target]
Alkyl-Chain
[References]
Chemical & Physical Properties
[ Density]:
1.0±0.1 g/cm3
[ Boiling Point ]:
309.2±25.0 °C at 760 mmHg
[ Molecular Formula ]:
C10H22N2O2
[ Molecular Weight ]:
202.294
[ Flash Point ]:
140.8±23.2 °C
[ Exact Mass ]:
202.168121
[ PSA ]:
64.35000
[ LogP ]:
1.29
[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C
[ Index of Refraction ]:
1.458
[ Storage condition ]:
2-8°C
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
C: Corrosive;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S36/37/39-S45
[ RIDADR ]:
UN 2735 8/PG 3
[ WGK Germany ]:
3
[ HS Code ]:
2924199090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2924199090
[ Summary ]:
2924199090. other acyclic amides (including acyclic 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. 32 , 79, (1989)
Several polymethylene tetraamines related to methoctramine (1) were prepared and evaluated for their blocking activity on M-2 muscarinic receptors in guinea pig atria and ileum. It turned out that ant...
T. Teshima et al.Tetrahedron 47 , 3305, (1991)
V.J. Jasys et al.
J. Org. Chem. 57 , 1814, (1992)