Benzophenone hydrazone - CAS 5350-57-2
Catalog: |
BB028248 |
Product Name: |
Benzophenone hydrazone |
CAS: |
5350-57-2 |
Synonyms: |
benzhydrylidenehydrazine |
IUPAC Name: | benzhydrylidenehydrazine |
Description: | Benzophenone hydrazone (CAS# 5350-57-2) is an intermediate used to synthesize Pseudobenztropine (P840155), an analog of Benzotropine (B207575, Mesylate salt) which is used as an antiparkinsonian.. It can also be used to prepare chiral [2.2]paracyclophane-substituted triazolium salts as precursors for copper-triazolylidene-catalyzed asymmetrical boration of unsaturated N-acyloxazolidinones. |
Molecular Weight: | 196.25 |
Molecular Formula: | C13H12N2 |
Canonical SMILES: | C1=CC=C(C=C1)C(=NN)C2=CC=CC=C2 |
InChI: | InChI=1S/C13H12N2/c14-15-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,14H2 |
InChI Key: | QYCSNMDOZNUZIT-UHFFFAOYSA-N |
Boiling Point: | 225-230 °C (55 mmHg) |
Appearance: | White to yellow powder |
MDL: | MFCD00007624 |
LogP: | 3.09800 |
Vapor Pressure: | 0.000151 [mmHg] |
GHS Hazard Statement: | H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P272, P273, P280, P301+P310, P302+P352, P321, P330, P333+P313, P363, P391, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113214096-A | Preparation and application of chiral quaternary ammonium salt | 20210513 |
CN-113209030-A | Preparation method of piperacillin sodium and tazobactam sodium sterile powder injection | 20210427 |
KR-20210032339-A | An organoelectro luminescent compounds and organoelectro luminescent device using the same | 20210305 |
CN-112645918-A | AIE type coumarin derivative fluorescent probe and application thereof in cyanide ion detection | 20201228 |
CN-112300178-A | Preparation and application of 5-bromoquinazoline derivative | 20201103 |
PMID | Publication Date | Title | Journal |
20672808 | 20100825 | N-H activation of hydrazines by iridium(I). Double N-H activation to form iridium aminonitrene complexes | Journal of the American Chemical Society |
20232925 | 20100416 | Two-step synthesis of substituted 3-aminoindazoles from 2-bromobenzonitriles | The Journal of organic chemistry |
14552764 | 20031103 | A general synthesis of 1-aryl carbamoyl-2-alkyl-4-aryl substituted semicarbazides as nonbasic factor Xa inhibitors | Bioorganic & medicinal chemistry letters |
11601651 | 20010801 | Improvement of the synthesis of diphenylmethyl 7beta-(o-hydroxy)benzylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate | Farmaco (Societa chimica italiana : 1989) |
11455650 | 20010201 | Synthesis and structure-activity relationships of benzophenone hydrazone derivatives with insecticidal activity | Pest management science |
Complexity: | 191 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 196.100048391 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 196.100048391 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 38.4 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.8 |
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