3-Hydroxy-4-nitrobenzaldehyde

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Names

[ CAS No. ]:
704-13-2

[ Name ]:
3-Hydroxy-4-nitrobenzaldehyde

[Synonym ]:
MFCD00007109
3-Hydroxy-4-nitrobenzaldehyde
Benzaldehyde, 3-hydroxy-4-nitro-
EINECS 211-879-7

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
303.3±27.0 °C at 760 mmHg

[ Melting Point ]:
127-131 °C(lit.)

[ Molecular Formula ]:
C7H5NO4

[ Molecular Weight ]:
167.119

[ Flash Point ]:
138.8±12.2 °C

[ Exact Mass ]:
167.021851

[ PSA ]:
83.12000

[ LogP ]:
1.67

[ Appearance of Characters ]:
yellow

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.667

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2913000090

Synthetic Route

Customs

[ HS Code ]: 2913000090

[ Summary ]:
HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0%

Articles

Tyrphostin AG126 exerts neuroprotection in CNS inflammation by a dual mechanism.

Glia 63(6) , 1083-99, (2015)

The putative protein tyrosine kinase (PTK) inhibitor tyrphostin AG126 has proven beneficial in various models of inflammatory disease. Yet molecular targets and cellular mechanisms remained enigmatic....

Catalytic enantioselective thioester aldol reactions that are compatible with protic functional groups.

J. Am. Chem. Soc. 127 , 7284, (2005)

This communication reports highly enantioselective and diastereoselective methyl malonic acid half thioester (MeMAHT) aldol reactions that are compatible with protic functional groups and enolizable a...

Characterization of a transient intermediate formed in the liver alcohol dehydrogenase catalyzed reduction of 3-hydroxy-4-nitrobenzaldehyde.

Biochemistry 26(11) , 3058-67, (1987)

The compounds 3-hydroxy-4-nitrobenzaldehyde and 3-hydroxy-4-nitrobenzyl alcohol are introduced as new chromophoric substrates for probing the catalytic mechanism of horse liver alcohol dehydrogenase (...


More Articles


Related Compounds

  • 2-ethoxy-3-hydroxy-4-nitrobenzaldehyde
  • 3-Hydroxy-4-methoxy-2-nitrobenzaldehyde
  • 3-hydroxy-4-oxobutyl-1-phosphonate
  • 3-Hydroxy-4-isopropylbenzoesaeuremethylester
  • 3-hydroxy-4-isopropyl-benzoic acid ethyl ester
  • 3-hydroxy-4-methyl-1,3-diphenyl-azetidin-2-one
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
  • N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine