3,5-DINITROBENZYL ALCOHOL

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Names

[ CAS No. ]:
71022-43-0

[ Name ]:
3,5-DINITROBENZYL ALCOHOL

[Synonym ]:
EINECS 275-131-1
(3,5-dinitrophenyl)methanol
MFCD00007235

Chemical & Physical Properties

[ Density]:
1.56g/cm3

[ Boiling Point ]:
404.2ºC at 760 mmHg

[ Melting Point ]:
88-91 °C(lit.)

[ Molecular Formula ]:
C7H6N2O5

[ Molecular Weight ]:
198.13300

[ Flash Point ]:
183.7ºC

[ Exact Mass ]:
198.02800

[ PSA ]:
111.87000

[ LogP ]:
2.04170

[ Index of Refraction ]:
1.641

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2906299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 3,5-Dinitrobenzoic acid
  • 3,5-Dinitrobenzoyl chloride
  • 1-(CHLOROMETHYL)-3,5-DINITROBENZENE
  • 3,5-Dinitrotoluene

DownStream

  • (3-Amino-5-nitrophenyl)methanol
  • 3-Chloro-5-fluorobenzaldehyde
  • (3-Amino-5-chlorophenyl)methanol
  • 3-chloro-5-fluorobenzyl alcohol
  • 1-(CHLOROMETHYL)-3,5-DINITROBENZENE
  • 3,5-DINITROBENZALDEHYDE
  • 1-(bromomethyl)-3,5-dinitrobenzene
  • 1,3-dinitro-5-(prop-2-enoxymethyl)benzene
  • 3-Chloro-5-nitrobenzaldehyde
  • 3,5-Dinitrophenylnitromethane

Customs

[ HS Code ]: 2906299090

[ Summary ]:
2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation.

Int. J. Nanomedicine 2 , 449-59, (2007)

The interaction of the important but often overdosed local anesthetic bupivacaine, its structural analogs 2,6-dimethylaniline, and N-methyl-2,6-dimethylacetanilide, and cocaine, with several electron ...

New ultraviolet labelling agents for high-performance liquid chromatographic determination of monocarboxylic acids.

J. Chromatogr. A. 481 , 211-9, (1989)

New UV-labelling agents have been synthesized, which are designed to convert monocarboxylic acids into their highly UV-absorbing derivatives for enhancement of the sensitivities of UV detection in hig...

Synthesis and characterization of hyperbranched polyurethanes prepared from blocked isocyanate monomers by step-growth polymerization. Spindler R and Frechet JMJ.

Macromolecules 26(18) , 4809-13, (1993)


More Articles

Related Compounds

  • 4-Methyl-3,5-dinitrobenzyl alcohol
  • 2-methyl-3,5-dinitrobenzyl alcohol
  • Vgl-DBE hydrochloride
  • 2-hydroxy-3-(2-hydroxy-3,5-dinitrobenzyl)tetrahydropyran
  • 3,5-Dichlorobenzyl alcohol
  • 3,5-DIMETHYLPHENETHYL ALCOHOL
  • (1R,2S)-1,2-Dibromo-3-chloro-1,2-dihydroacenaphthylene
  • 1,1-Diethyl 2-hydroxy-1,1-cyclohexanedicarboxylate
  • 4-(3-Methoxyphenyl)-2,5-dihydrofuran-2-one
  • 1-(2,3-Dimethylphenyl)pentan-1-amine
  • Phenyl(3,4,6-trimethyl-3-cyclohexen-1-yl)methanone
  • 1,1,1,4,4-Pentachloro-3-buten-2-one
  • 1-(4-(Chloromethyl)phenyl)-2-methyl-1H-benzo[d]imidazole
  • 4-Butyl-1,2-difluorobenzene
  • 1-[Bis(1-methylethyl)amino]-3-(2-furanylmethoxy)-2-propanol
  • (2-Ethylcyclopentyl)methanamine hydrochloride
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