tert-Butyl [(4-methylphenyl)sulfonyl]carbamate structure
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Common Name | tert-Butyl [(4-methylphenyl)sulfonyl]carbamate | ||
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CAS Number | 18303-04-3 | Molecular Weight | 271.333 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | N/A | |
Molecular Formula | C12H17NO4S | Melting Point | 121-123ºC(lit.) | |
MSDS | Chinese USA | Flash Point | N/A |
Name | tert-butyl N-(4-methylphenyl)sulfonylcarbamate |
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Synonym | More Synonyms |
Density | 1.2±0.1 g/cm3 |
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Melting Point | 121-123ºC(lit.) |
Molecular Formula | C12H17NO4S |
Molecular Weight | 271.333 |
Exact Mass | 271.087830 |
PSA | 80.85000 |
LogP | 2.56 |
Index of Refraction | 1.522 |
Water Solubility | chloroform: soluble25mg/mL, clear, colorless |
Safety Phrases | 24/25 |
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RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2935009090 |
~96% tert-Butyl [(4-... CAS#:18303-04-3 |
Literature: Nouria, Azita; Akbari, Jafar; Heydaric, Akbar; Nouri, Arezu Letters in Organic Chemistry, 2011 , vol. 8, # 1 p. 38 - 42 |
~96% tert-Butyl [(4-... CAS#:18303-04-3 |
Literature: Moore, Joel D; Harned, Andrew M; Henle, Julia; Flynn, Daniel L; Hanson, Paul R Organic letters, 2002 , vol. 4, # 11 p. 1847 - 1849 |
~95% tert-Butyl [(4-... CAS#:18303-04-3 |
Literature: Johnson II, David C.; Widlanski, Theodore S. Tetrahedron Letters, 2004 , vol. 45, # 46 p. 8483 - 8487 |
~% tert-Butyl [(4-... CAS#:18303-04-3 |
Literature: Tetrahedron Letters, , vol. 45, # 46 p. 8483 - 8487 |
~% tert-Butyl [(4-... CAS#:18303-04-3 |
Literature: Tetrahedron Letters, , vol. 45, # 46 p. 8483 - 8487 |
~% tert-Butyl [(4-... CAS#:18303-04-3 |
Literature: Tetrahedron Letters, , vol. 45, # 46 p. 8483 - 8487 |
Precursor 6 | |
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DownStream 10 | |
HS Code | 2935009090 |
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Summary | 2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0% |
Tetrahedron Lett. 30 , 5709, (1989)
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Use of the Mitsunobu reaction in the synthesis of orthogonally protected a, ß-diaminopropionic acids. Kelleher F.
Tetrahedron Lett. 48(28) , 4879-82, (2007)
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Diastereoselective formal synthesis of a monoterpene alkaloid, (-)-incarvilline.
J. Org. Chem. 72(17) , 6541-7, (2007) Diastereoselective formal synthesis of a monoterpene alkaloid, (-)-incarvilline, the key intermediate for the synthesis of (-)-incarvillateine, was achieved by using an intramolecular Pauson-Khand rea... |
Weinreb's reagent |
tert-butyl tosylcarbamate |
N-Boc p-toluenesufonamide |
tert-Butyl [(4-methylphenyl)sulfonyl]carbamate |
N-Boc-N-tosylamide |
2-Methyl-2-propanyl [(4-methylphenyl)sulfonyl]carbamate |
N-(tert-Butoxycarbonyl)-p-toluenesulfonaMide |
N-Boc-p-toluenesulfonamide |
Carbamic acid, N-[(4-methylphenyl)sulfonyl]-, 1,1-dimethylethyl ester |
N-tosyl-N-Boc amide |
N-Boc-N-tosylamine |
MFCD00134267 |