Di-tert-Butyl azodicarboxylate structure
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Common Name | Di-tert-Butyl azodicarboxylate | ||
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CAS Number | 870-50-8 | Molecular Weight | 230.261 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 287.1±9.0 °C at 760 mmHg | |
Molecular Formula | C10H18N2O4 | Melting Point | 89-92 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 107.2±13.2 °C | |
Symbol |
GHS08 |
Signal Word | Danger |
Name | Di-tert-Butyl azodicarboxylate |
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Synonym | More Synonyms |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 287.1±9.0 °C at 760 mmHg |
Melting Point | 89-92 °C(lit.) |
Molecular Formula | C10H18N2O4 |
Molecular Weight | 230.261 |
Flash Point | 107.2±13.2 °C |
Exact Mass | 230.126663 |
PSA | 77.32000 |
LogP | 3.24 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.460 |
Storage condition | 2-8°C |
Water Solubility | Insoluble |
Symbol |
GHS08 |
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Signal Word | Danger |
Hazard Statements | H360FD |
Precautionary Statements | P201-P308 + P313 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | F:Flammable;Xi:Irritant; |
Risk Phrases | R11;R36/37/38 |
Safety Phrases | S26-S36-S37/39-S16 |
RIDADR | 1325 |
WGK Germany | 3 |
RTECS | VZ2275000 |
HS Code | 2927000090 |
~98% Di-tert-Butyl a... CAS#:870-50-8 |
Literature: Juermann, Gea; Tsubrik, Olga; Tammeveski, Kaido; Maeeorg, Uno Journal of Chemical Research, 2005 , # 10 p. 661 - 662 |
~% Di-tert-Butyl a... CAS#:870-50-8 |
Literature: Journal of the American Chemical Society, , vol. 134, # 45 p. 18581 - 18584 |
~% Di-tert-Butyl a... CAS#:870-50-8 |
Literature: Tetrahedron Letters, , vol. 43, # 35 p. 6213 - 6215 |
Precursor 3 | |
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DownStream 7 | |
HS Code | 2927000090 |
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Summary | 2927000090 other diazo-, azo- or azoxy-compounds。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0% |
Axially chiral guanidine as highly active and enantioselective catalyst for electrophilic amination of unsymmetrically substituted 1,3-dicarbonyl compounds.
J. Am. Chem. Soc. 128 , 16044, (2006) A newly designed axially chiral guanidine is found to function as an effective platform for asymmetric induction at the alpha-carbon of unsymmetrically substituted 1,3-dicarbonyl compounds. Highly eff... |
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Chirally aminated 2-naphthols--organocatalytic synthesis of non-biaryl atropisomers by asymmetric Friedel-Crafts amination.
Angew. Chem. Int. Ed. Engl. 45(7) , 1147-1151, (2006)
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Catalytic Enantioselective Reaction of α-Aminoacetonitriles Using Chiral Bis(imidazoline) Palladium Catalysts.
Angew. Chem. Int. Ed. Engl. 54(28) , 8198-202, (2015) The catalytic enantioselective reaction of diphenylmethylidene-protected α-aminoacetonitriles with imines has been developed. Good yields and diastereo- and enantioselectivities were observed for the ... |
di-tert-butylazodicarboxylate |
EINECS 212-796-9 |
MFCD00015001 |
Bis(2-methyl-2-propanyl) 1,2-diazenedicarboxylate |
Boc-N=N-Boc |
Di-tert-Butyl azodic |
tert-butyl azodicarboxylate |
di-tert-butylazadicarboxylate |
Di-tert-butyl azodicarboxylate |
DI-TERT-BUTYL AZODICARBOXYALTE |
DI-T-BUTYL AZODICARBOXYLATE |
tBuO2CN=NCO2tBu |
1,2-Diazenedicarboxylic acid, bis(1,1-dimethylethyl) ester |
Di-tert-butyl diazene-1,2-dicarboxylate |