Di-tert-butyl iminodicarboxylate
Di-tert-butyl iminodicarboxylate structure
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Common Name | Di-tert-butyl iminodicarboxylate | ||
|---|---|---|---|---|
| CAS Number | 51779-32-9 | Molecular Weight | 217.26 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 273.8±9.0 °C at 760 mmHg | |
| Molecular Formula | C10H19NO4 | Melting Point | 114-117 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 119.4±18.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of Di-tert-butyl iminodicarboxylateDi-tert-butyl iminodicarboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | Di-tert-butyl iminodicarboxylate |
|---|---|
| Synonym | More Synonyms |
| 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 | |
| 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。 |
| 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 |
| 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 |
|
~53%
Di-tert-butyl i... CAS#:51779-32-9 |
| Literature: Bunnenberg, Rolf; Jochims, Johannes C. Chemische Berichte, 1981 , vol. 114, # 6 p. 2064 - 2074 |
|
~%
Di-tert-butyl i... CAS#:51779-32-9 |
| Literature: Abramovitch,R.A. et al. Journal of Organic Chemistry, 1974 , vol. 39, p. 2513 - 2516 |
|
~%
Di-tert-butyl i... CAS#:51779-32-9 |
| Literature: Carpino,L.A. Journal of Organic Chemistry, 1964 , vol. 29, p. 2820 - 2824 |
|
~0%
Di-tert-butyl i... CAS#:51779-32-9 |
| Literature: Allan, Robin D.; Johnston, Graham A. R.; Kazlauskas, Rymantas; Tran, Hue W. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1983 , # 12 p. 2983 - 2986 |
|
~%
Di-tert-butyl i... CAS#:51779-32-9 |
| Literature: Grehn, Leif; Ragnarsson, Ulf Synthesis, 1987 , # 3 p. 275 - 276 |
|
~%
Di-tert-butyl i... CAS#:51779-32-9 |
| Literature: Carpino,L.A. Journal of Organic Chemistry, 1964 , vol. 29, p. 2820 - 2824 |
|
~%
Di-tert-butyl i... CAS#:51779-32-9 |
| Literature: Clarke,C.T. et al. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1978 , p. 1088 - 1090 |
![5-(2-bromoethylidene)-4-[(2-methylpropan-2-yl)oxy]furan-2-one structure](https://image.chemsrc.com/caspic/381/89004-80-8.png)
| Precursor 10 | |
|---|---|
| DownStream 10 | |
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CAS#:202925-92-6| 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% |
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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... |
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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 ... |
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A convenient and efficient synthesis of (< i> S</i>)-lysine and (< i> S</i>)-arginine homologues via olefin cross-metathesis. Boyle TP, et al.
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| 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 |
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