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5-Nitro-1,3-benzoxazole

CAS No.
70886-33-8
Chemical Name:
5-Nitro-1,3-benzoxazole
Synonyms
5-Nitrobenzoxazole;Benzoxazole, 5-nitro-;5-Nitro-1,3-benzoxazole
CBNumber:
CB5154128
Molecular Formula:
C7H4N2O3
Molecular Weight:
164.12
MDL Number:
MFCD01359855
MOL File:
70886-33-8.mol
MSDS File:
SDS
Last updated:2026-09-12 18:53:14

5-Nitro-1,3-benzoxazole Properties

Melting point 127-129°
Boiling point 294.2±13.0 °C(Predicted)
Density 1.473±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka -5.69±0.10(Predicted)
Appearance Light yellow to brown Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H320-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
HazardClass  IRRITANT
HS Code  2934999090

5-Nitro-1,3-benzoxazole price More Price(40)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific OR60169 5-Nitro-1,3-benzoxazole ≥95% 70886-33-8 1g $21 2026-06-04 Buy
Apolloscientific OR60169 5-Nitro-1,3-benzoxazole ≥95% 70886-33-8 5g $48 2026-06-04 Buy
Matrix Scientific 045160 5-Nitro-1,3-benzoxazole 70886-33-8 10.00g $65 2026-05-18 Buy
Matrix Scientific 045160 5-Nitro-1,3-benzoxazole 70886-33-8 25.00g $160 2026-05-18 Buy
Matrix Scientific 045160 5-Nitro-1,3-benzoxazole 70886-33-8 100.00g $628 2026-05-18 Buy
Product number Packaging Price Buy
OR60169 1g $21 Buy
OR60169 5g $48 Buy
045160 10.00g $65 Buy
045160 25.00g $160 Buy
045160 100.00g $628 Buy

5-Nitro-1,3-benzoxazole Chemical Properties,Uses,Production

Uses

5-Nitrobenzoxazole is a useful reactant for copper-catalyzed direct carboxylation of C-H bonds in benzoxazoles and related compounds with carbon dioxide.

Synthesis

Triethyl orthoformate

122-51-0

2-Amino-4-nitrophenol

99-57-0

5-NITRO-1,3-BENZOXAZOLE

70886-33-8

To a 50 mL single-necked round-bottomed flask equipped with a magnetic stirrer was added 2-amino-4-nitrophenol (5.0 mmol, 1.0 eq.) and triethyl orthoformate (60.0 mmol, 12.0 eq.). The reaction mixture was slowly heated to 150 °C and the reaction was stirred at this temperature for 6 hours. Upon completion of the reaction, the mixture was cooled to room temperature, followed by distillation under reduced pressure to remove the excess triethyl orthoformate and the resulting ethanol by-product. The crude product was purified by silica gel column chromatography to give the final target compound 5-nitrobenzoxazole (see Table S-2).

References

[1] Angewandte Chemie - International Edition, 2011, vol. 50, # 48, p. 11511 - 11515
[2] Journal of the Chinese Chemical Society, 2015, vol. 62, # 5, p. 412 - 419
[3] Tetrahedron, 2013, vol. 69, # 32, p. 6627 - 6633
[4] Comptes Rendus Chimie, 2013, vol. 16, # 11, p. 1029 - 1034
[5] Angewandte Chemie - International Edition, 2009, vol. 48, # 48, p. 9127 - 9130

5-Nitro-1,3-benzoxazole Preparation Products And Raw materials

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Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60

5-Nitro-1,3-benzoxazole Spectrum

5-Nitrobenzoxazole Benzoxazole, 5-nitro- 5-Nitro-1,3-benzoxazole 70886-33-8