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159217-89-7

159217-89-7 Structure

159217-89-7 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE
[CAS]

159217-89-7
[Synonyms]

N-BOC-4-IODOANILINE
TERT-BUTYL 4-IODOPHENYLCARBAMATE
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE
N-(tert-Butoxycarbonyl)-4-iodoaniline
(4-Iodophenyl)carbamic acid tert-butyl ester
N-(4-iodophenyl)carbamic acid tert-butyl ester
Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C11H14INO2
[MDL Number]

MFCD03490497
[MOL File]

159217-89-7.mol
[Molecular Weight]

319.14
Chemical PropertiesBack Directory
[Melting point ]

146-147°C
[Boiling point ]

299.0±23.0 °C(Predicted)
[density ]

1.591±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[pka]

13.12±0.70(Predicted)
[Appearance]

White to off-white Solid
[Sensitive ]

Light Sensitive
[InChI]

1S/C11H14INO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14)
[InChIKey]

CGALRQWBJFDAKN-UHFFFAOYSA-N
[SMILES]

CC(C)(C)OC(=O)Nc1ccc(I)cc1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302-H317-H410
[Precautionary statements ]

P261-P264-P273-P280-P301+P312-P302+P352
[Hazard Codes ]

Xn,N
[Risk Statements ]

22-43-50
[Safety Statements ]

36/37-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
[HS Code ]

2924297099
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Skin Sens. 1
Spectrum DetailBack Directory
[Spectrum Detail]

TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE(159217-89-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

4-Iodoaniline

540-37-4

TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE

159217-89-7

GENERAL STEPS: The reaction was carried out in a 50 mL round-bottomed flask at 80°C under reduced pressure for 10 minutes. In a typical experiment, 5 mmol of p-iodoaniline was mixed with 5 mmol of di-tert-butyl dicarbonate and the reaction lasted for 10 minutes. Upon completion of the reaction, the solvent was removed by rotary evaporator under vacuum to give tert-butyl (4-iodophenyl)carbamate.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 22, p. 5864 - 5869
[2] Research on Chemical Intermediates, 2017, vol. 43, # 3, p. 1355 - 1363
[3] Chemical Communications, 2013, vol. 49, # 61, p. 6909 - 6911
[4] Patent: WO2004/12736, 2004, A1. Location in patent: Page/Page column 24
[5] Organic Letters, 2018, vol. 20, # 7, p. 1693 - 1697
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