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56301-51-0

N-benzylphenothiazine radical cation is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56301-51-0 Structure

  • Basic information

    1. Product Name: N-benzylphenothiazine radical cation
    2. Synonyms:
    3. CAS NO:56301-51-0
    4. Molecular Formula:
    5. Molecular Weight: 289.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56301-51-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-benzylphenothiazine radical cation(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzylphenothiazine radical cation(56301-51-0)
    11. EPA Substance Registry System: N-benzylphenothiazine radical cation(56301-51-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 56301-51-0(Hazardous Substances Data)

56301-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56301-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,0 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56301-51:
(7*5)+(6*6)+(5*3)+(4*0)+(3*1)+(2*5)+(1*1)=100
100 % 10 = 0
So 56301-51-0 is a valid CAS Registry Number.

56301-51-0Upstream product

56301-51-0Downstream Products

56301-51-0Relevant articles and documents

One-electron oxidation of N-benzylphenothiazine by nitric acid in the presence of β-cyclodextrin

Zhang, Hai-Ming,Ruan, Xiu-Qin,Guo, Qing-Xiang,Liu, You-Cheng

, p. 449 - 450 (1998)

Oxidation of N-benzylphenothiazine with nitric acid in aqueous solution was investigated in the presence of β-cyclodextrin by means of UV-vis and ESR spectroscopy. The N-benzylphenothiazine radical cation generated in β-cyclodextrin cavity is much more st

Electron transfer between n-substituted phenothiazines and the 1- oxopiperidinium ion in the presence of β-cyclodextrin

Zheng, Xiao-Qi,Ruan, Xiu-Qin,Wang, Wei,Zhang, Hai-Ming,Guo, Qing-Xiang,Liu, You-Cheng

, p. 253 - 257 (1999)

The electron-transfer reactions between N-substituted phenothiazines and 4-acetoxy-2,2,6,6-tetramethyl-1-oxopiperidinium hexachloroantimonate (ATPO) in the presence of β-cyclodextrin (β-CD) in an aqueous solution have been studied. N-phenylphenothiazine (

Interaction of N-substituted phenothiazines with halogen-containing solvents

Tomilin,Konovalova,Yuzhalkin,Klyakin,Sanaeva

, p. 246 - 248 (2007/10/03)

ESR spectroscopy was used to study the interaction of several N-substituted phenothiazines with halogen-containing solvents (CCl4, CHCl3, CH2Br2). The dissolution of phenothiazines in these solvents was found to be associated with an ESR signal indicating the presence of an oxidation-reduction reaction in which the halogen-containing compounds act as acceptors, and the phenothiazines act as electron donors. The HFS of the ESR spectra of the cation radicals obtained was studied. 1996 Plenum Publishing Corporation.

Endor Studies of Cation Radicals from Pharmacologically Active Phenothiazines

Helle, N.,Kurreck, H.,Bock, M.,Kieslich, W.

, p. 964 - 970 (2007/10/02)

A variety of substituted phenothiazine cation radicals, including those from pharmacologically active derivatives, e.g. chloropromazine, alimemazine and laevomepromazine, have been studied by means of ENDOR and TRIPLE resonace spectroscopy.These techniques allowed accurate determinations of hyperfine coupling constants, including their signs.Conclusions concerning molecular structure (e.g. twist angles) could be drawn, supporting previous investigations of the interrelationship of molecular conformations with the pharmacological potential, i.e. neuroleptic, antihistaminic or anti-Parkinsonian.

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