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TERT-BUTYL (4-NITROBENZYL)CARBAMATE

CAS No.
94838-58-1
Chemical Name:
TERT-BUTYL (4-NITROBENZYL)CARBAMATE
Synonyms
N-Boc-4-nitrobenzylamine;TERT-BUTYL (4-NITROBENZYL)CARBAMATE;2-Methyl-2-propanyl (4-nitrobenzyl)carbamate;tert-butyl N-[(4-nitrophenyl)methyl]carbamate;Carbamic acid, N-[(4-nitrophenyl)methyl]-, 1,1-dimethylethyl ester
CBNumber:
CB8835552
Molecular Formula:
C12H16N2O4
Molecular Weight:
252.27
MDL Number:
MFCD09038178
MOL File:
94838-58-1.mol
MSDS File:
SDS
Last updated:2026-05-28 06:16:00

TERT-BUTYL (4-NITROBENZYL)CARBAMATE Properties

Melting point 105-108 °C
Boiling point 408.8±28.0 °C(Predicted)
Density 1.187±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 11.58±0.46(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

TERT-BUTYL (4-NITROBENZYL)CARBAMATE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth UDA83858 tert-Butyl 4-nitrobenzylcarbamate 94838-58-1 10g $354 2026-06-05 Buy
aablocks AA0067FZ tert-Butyl 4-nitrobenzylcarbamate 95% 94838-58-1 1g $20 2026-05-28 Buy
aablocks AA0067FZ tert-Butyl 4-nitrobenzylcarbamate 95% 94838-58-1 5g $68 2026-05-28 Buy
aablocks AA0067FZ tert-Butyl 4-nitrobenzylcarbamate 98% 94838-58-1 25g $274 2026-05-28 Buy
aablocks AA0067FZ tert-Butyl 4-nitrobenzylcarbamate 98% 94838-58-1 100g $940 2026-05-28 Buy
Product number Packaging Price Buy
UDA83858 10g $354 Buy
AA0067FZ 1g $20 Buy
AA0067FZ 5g $68 Buy
AA0067FZ 25g $274 Buy
AA0067FZ 100g $940 Buy

TERT-BUTYL (4-NITROBENZYL)CARBAMATE Chemical Properties,Uses,Production

Synthesis

Di-tert-butyl dicarbonate

24424-99-5

4-Nitrobenzylamine hydrochloride

18600-42-5

TERT-BUTYL (4-NITROBENZYL)CARBAMATE

94838-58-1

Step 1: Preparation of tert-butyl 4-nitrobenzylcarbamate (C4) 4-Nitrobenzylamine hydrochloride (10 g, 53.0 mmol) was suspended in a mixed solvent of THF (150 mL) and water (13 mL) and cooled to 0 °C. Di-tert-butyl dicarbonate (11.6 g, 53.0 mmol) and N,N-diisopropylethylamine (27.7 mL, 159 mmol) were added sequentially under stirring. The reaction mixture was stirred at 0 °C for 30 min and then slowly warmed up to 25 °C and continued stirring for about 20 hours. Upon completion of the reaction, most of the THF was removed by concentration under reduced pressure. the residue was dissolved in EtOAc and washed sequentially with 1N HCl, saturated NaHCO3 solution and saturated NaCl solution. The organic phase was dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give the off-white solid product C4 (14.0 g, 99% yield). 1H NMR (400 MHz, d6-DMSO) δ: 8.16 (d, 2H), 7.55 (t, 1H), 7.46 (d, 2H), 4.21 (d, 2H), 1.36 (s, 9H).

References

[1] Patent: US2009/54395, 2009, A1. Location in patent: Page/Page column 48
[2] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 24, p. 4389 - 4393
[3] European Journal of Medicinal Chemistry, 2014, vol. 80, p. 101 - 111
[4] Chemical Communications, 2014, vol. 50, # 97, p. 15305 - 15308
[5] Patent: US2016/264520, 2016, A1. Location in patent: Paragraph 0332; 0333; 0334; 0335

TERT-BUTYL (4-NITROBENZYL)CARBAMATE Preparation Products And Raw materials

Global( 31)Suppliers
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Shanghai Joiny Pharmaceutical Co.,Ltd. 13681955282 gyd@joiny-pharma.com China 431 58
TERT-BUTYL (4-NITROBENZYL)CARBAMATE tert-butyl N-[(4-nitrophenyl)methyl]carbamate N-Boc-4-nitrobenzylamine Carbamic acid, N-[(4-nitrophenyl)methyl]-, 1,1-dimethylethyl ester 2-Methyl-2-propanyl (4-nitrobenzyl)carbamate 94838-58-1