2-(Trifluoromethyl)phenylhydrazine Hydrochloride - CAS 3107-34-4
Catalog: |
BB020791 |
Product Name: |
2-(Trifluoromethyl)phenylhydrazine Hydrochloride |
CAS: |
3107-34-4 |
Synonyms: |
[2-(trifluoromethyl)phenyl]hydrazine;hydrochloride; [2-(trifluoromethyl)phenyl]hydrazine;hydrochloride |
IUPAC Name: | [2-(trifluoromethyl)phenyl]hydrazine;hydrochloride |
Description: | 2-(Trifluoromethyl)phenylhydrazine Hydrochloride (CAS# 3107-34-4) is a useful research chemical. |
Molecular Weight: | 212.60 |
Molecular Formula: | C7H8ClF3N2 |
Canonical SMILES: | C1=CC=C(C(=C1)C(F)(F)F)NN.Cl |
InChI: | InChI=1S/C7H7F3N2.ClH/c8-7(9,10)5-3-1-2-4-6(5)12-11;/h1-4,12H,11H2;1H |
InChI Key: | ZUSWDTWYONAOPH-UHFFFAOYSA-N |
Boiling Point: | 196.1 °C at 760 mmHg |
Density: | 1.505 g/cm3 |
Solubility: | 15.7 [ug/mL] (The mean of the results at pH 7.4) |
MDL: | MFCD00102619 |
LogP: | 3.56630 |
GHS Hazard Statement: | H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
US-2020131154-A1 | Pyrazolyl compounds and methods of use thereof | 20181026 |
US-2019152896-A1 | Continuous Flow Process For the Synthesis of Phenylhydrazine Salts and Substituted Phenylhydrazine Salts | 20160727 |
US-11040938-B2 | Continuous flow process for the synthesis of phenylhydrazine salts and substituted phenylhydrazine salts | 20160727 |
EP-3464268-A1 | Novel compounds | 20160531 |
WO-2017207432-A1 | Novel compounds | 20160531 |
PMID | Publication Date | Title | Journal |
22838405 | 20120907 | Studies on the selectivity between nickel-catalyzed 1,2-cis-2-amino glycosylation of hydroxyl groups of thioglycoside acceptors with C2-substituted benzylidene N-phenyl trifluoroacetimidates and intermolecular aglycon transfer of the sulfide group | The Journal of organic chemistry |
21360410 | 20110201 | Microwave-assisted synthesis of 2(1H)-pyridones and their glucosides as cell proliferation inhibitors | Nucleosides, nucleotides & nucleic acids |
20000685 | 20100310 | Synthesis of 4-methyl-1,2,3-thiadiazole derivatives via Ugi reaction and their biological activities | Journal of agricultural and food chemistry |
15210150 | 20040715 | Synthesis and biological evaluation of 1,4-dihydropyridine calcium channel modulators having a diazen-1-ium-1,2-diolate nitric oxide donor moiety for the potential treatment of congestive heart failure | Bioorganic & medicinal chemistry |
Complexity: | 146 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 212.0328104 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 5 |
Hydrogen Bond Donor Count: | 3 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 212.0328104 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 38 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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