NH2-C4-NH-Boc
Names
[ CAS No. ]:
68076-36-8
[ Name ]:
NH2-C4-NH-Boc
[Synonym ]:
2-Methyl-2-propanyl (4-aminobutyl)carbamate
BOC-NH(CH2)4NH2 HCL
tert-butyl 4-aminobutylcarbamate
Carbamic acid, N-(4-aminobutyl)-, 1,1-dimethylethyl ester
(4-amino-butyl)-carbamic acid tert-butyl ester
N-(1,1-dimethylethoxycarbonyl)-1,4-butanediamine
BOC-DIAMINOBUTANE HCL
N-Boc-1,4-butanediamine
N-Boc-1,4-butandiamine
N-T-BOC-BUTANDIAMINE HCL
(4-aminobutyl)carbamic acid 1,1-dimethylethyl ester
BUTTPARK 121 6-09
RARECHEM AR PA 0023
tert-ButylN-(4-aminobutyl)carbamate
4-(t-butoxycarbonylamino)butylamine
N-BOC-1,4-DIAMINOBUTANE
AURORA KA-4397
N-(tert-butoxycarbonyl)-1,4-diamino-butane
BOC-DAB HCL
N-tert-Butoxycarbonyl-1,4-butanediamine
MFCD02090802
tert-butyl 4-amino butylcarbamate
Biological Activity
[Description]:
[Related Catalog]:
[Target]
Alkyl/ether
[References]
Chemical & Physical Properties
[ Density]:
1.0±0.1 g/cm3
[ Boiling Point ]:
292.9±23.0 °C at 760 mmHg
[ Molecular Formula ]:
C9H20N2O2
[ Molecular Weight ]:
188.267
[ Flash Point ]:
130.9±22.6 °C
[ Exact Mass ]:
188.152481
[ PSA ]:
64.35000
[ LogP ]:
1.06
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.457
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
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S36/37/39-S45
[ RIDADR ]:
UN 2735 8/PG 3
[ WGK Germany ]:
3
[ Hazard Class ]:
8.0
[ HS Code ]:
2924199090
Synthetic Route
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
Biopolymers 104 , 206-12, (2015)
Recently, we described a process of trypsin-assisted peptide splicing of analogs of trypsin inhibitor SFTI-1, that seems to be very similar to proteasome-catalyzed peptide splicing. Here, we show, for...
Synthesis, tubulin binding, antineoplastic evaluation, and structure-activity relationship of oncodazole analogues.J. Med. Chem. 32 , 409, (1989)
In an attempt to identify a soluble oncodazole analogue that could be easily formulated, a series of substituted oncodazoles was synthesized and evaluated for tubulin binding affinity, in vitro cytoto...
Synthesis and biological evaluation of new citrate-based siderophores as potential probes for the mechanism of iron uptake in mycobacteria.J. Med. Chem. 45 , 2056, (2002)
Several iron chelators containing alpha,beta-unsaturated hydroxamic acid motifs appended to a citric acid platform were synthesized. Mycobacterium paratuberculosis was then challenged to grow in the p...