Di-tert-butyl iminodicarboxylate

Names

[ Name ]:
Di-tert-butyl iminodicarboxylate

[Synonym ]:
tert-butyl N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate
Di-t-butyl iminodicarboxylate
Carbamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1,1-dimethylethyl ester
tert-Butyl iminodicarboxylate
Bis(2-methyl-2-propanyl) imidodicarbonate
di-tert-butyl imidodicarbonate
N-Boc-tert-butylcarbamate
MFCD00043309
Iminodicarboxylic Acid Di-tert-butyl Ester
Di-tert-butyl-iminodicarboxylate
Di-tert-butylimino dicarboxylate

Biological Activity

[Description]:

Di-tert-butyl iminodicarboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

[In Vitro]

Di-tert-butyl-iminodicarboxylate 可用于制备反式-二氨基-2-丁烯和顺式-1,4-二氨基-2-丁烯； N-3-丁烯基亚氨基二羧酸二叔丁酯； N,N-二叔丁基[(2-氟-4-硝基)苄基氨基]二羧酸酯和四纤维蛋白的 C1-C20 和 C21-C40 片段。改良的 Gabriel 试剂。

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
273.8±9.0 °C at 760 mmHg

[ Melting Point ]:
114-117 °C(lit.)

[ Molecular Formula ]:
C₁₀H₁₉NO₄

[ Molecular Weight ]:
217.26

[ Flash Point ]:
119.4±18.7 °C

[ Exact Mass ]:
217.131409

[ PSA ]:
64.63000

[ LogP ]:
2.25

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.442

[ Storage condition ]:
2-8°C

MSDS

Click to get detail 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-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925290090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2925290090

[ Summary ]:
2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Synthesis, biological evaluation and molecular modeling studies of N6-benzyladenosine analogues as potential anti-toxoplasma agents.

Biochem. Pharmacol. 73 , 1558-1572, (2007)

Toxoplasma gondii is an opportunistic pathogen responsible for toxoplasmosis. T. gondii is a purine auxotroph incapable of de novo purine biosynthesis and depends on salvage pathways for its purine re...

Identification of the putrescine recognition site on polyamine transport protein PotE.

J. Biol. Chem. 275(46) , 36007-12, (2000)

The PotE protein can catalyze both uptake and excretion of putrescine. The K(m) values of putrescine for uptake and excretion are 1.8 and 73 microm, respectively. Uptake of putrescine is dependent on ...

A convenient and efficient synthesis of (< i> S</i>)-lysine and (< i> S</i>)-arginine homologues via olefin cross-metathesis. Boyle TP, et al.

Tetrahedron 61(30) , 7271-76, (2005)