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Benzeneacetaldehyde, a-phenyl-, oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 41401-03-0 Structure
  • Basic information

    1. Product Name: Benzeneacetaldehyde, a-phenyl-, oxime
    2. Synonyms:
    3. CAS NO:41401-03-0
    4. Molecular Formula: C14H13NO
    5. Molecular Weight: 211.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41401-03-0.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: Benzeneacetaldehyde, a-phenyl-, oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetaldehyde, a-phenyl-, oxime(41401-03-0)
    11. EPA Substance Registry System: Benzeneacetaldehyde, a-phenyl-, oxime(41401-03-0)
  • 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: 41401-03-0(Hazardous Substances Data)

41401-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41401-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,0 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41401-03:
(7*4)+(6*1)+(5*4)+(4*0)+(3*1)+(2*0)+(1*3)=60
60 % 10 = 0
So 41401-03-0 is a valid CAS Registry Number.

41401-03-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenyl-acetaldehyde-oxime

1.2 Other means of identification

Product number -
Other names Diphenyl-acetaldehyd-oxim

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:41401-03-0 SDS

41401-03-0Relevant articles and documents

1,2,4-Oxadiazolidin-3,5-diones and 1,3,5-triazin-2,4,6-triones as cytosolic phospholipase A2α inhibitors

Gopalsamy, Ariamala,Yang, Hui,Ellingboe, John W.,McKew, John C.,Tam, Steve,Joseph-McCarthy, Diane,Zhang, Wen,Shen, Marina,Clark, James D.

, p. 2978 - 2981 (2008/09/21)

1,2,4-Oxadiazolidin-3,5-dione and 1,3,5-triazin-2,4,6-trione scaffolds were employed as templates to incorporate the pharmacophore requirements of cytosolic phospholipase A2α substrate mimetics. Inhibitors that are active in both enzyme, and ce

One-pot copper(I)-catalyzed synthesis of 3,5-disubstituted isoxazoles

Hansen, Trond V.,Wu, Peng,Fokin, Valery V.

, p. 7761 - 7764 (2007/10/03)

3,5-Disubstituted isoxazoles are obtained in good yields by a convenient one-pot, three-step procedure utilizing a regioselective copper(I)-catalyzed cycloaddition reaction between in situ generated nitrile oxides and terminal acetylenes. Most functional

Titanium(III) Chloride Mediated Reduction of 1-Nitro-2-phenylethenes

Sera, Akira,Fukumoto, Shoji,Tamura, Masako,Takabatake, Kiyoshi,Yamada, Hiroaki,Itoh, Kuniaki

, p. 1787 - 1791 (2007/10/02)

The reaction of 1-nitro-2-phenylethenes (β-nitrostyrenes) with aqueous titanium(III) chloride afforded substituted pyrroles in addition to the expected reduction products, oximes and carbonyl compounds. 2-Substituted 1-nitro-2-phenylethenes yielded divinylamine derivatives instead of pyrroles.The reaction mechanism has been rationalized by taking account of the electron transfer from titanium(III) species to the nitro olefines, followed by protonation, dimerization, cyclization, and/or hydrolysis.

TITANIUM TRICHLORIDE MEDIATED REDUCTION OF NITROSTYRENES

Sera, Akira,Fukumoto, Shoji,Yoneda, Takako,Yamada, Hiroaki

, p. 697 - 702 (2007/10/02)

Reactions of substituted nitrostyrenes with aqueous titanium trichloride afforded pyrroles, carbonyl compounds, and oximes.In some instances, divinylamines were produced as well.The reaction mechanism is rationalized taking account of electron transfer to nitroethylenes from Ti(III), followed by protonation, dimerization, cyclization, and hydrolysis.

Photochemical and Chemical Reduction of Nitroalkenes Using Viologens as an Electron Phase-Transfer Catalyst

Tomioka, Hideo,Ueda, Koichi,Ohi, Hirofumi,Izawa, Yasuji

, p. 1359 - 1362 (2007/10/02)

An amphiphilic electron acceptor, i.e., N,N'-dioctyl-4,4'-bipyridinium, was used as an electron carrier between water-oil two phase, in which nitroalkenes in organic phase were readily reduced to the corresponding oximes and/or carbonyl compounds.

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