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Hydrazine, 1-phenyl-1-(2-propynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61944-48-7

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61944-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61944-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,4 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61944-48:
(7*6)+(6*1)+(5*9)+(4*4)+(3*4)+(2*4)+(1*8)=137
137 % 10 = 7
So 61944-48-7 is a valid CAS Registry Number.

61944-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-1-prop-2-ynylhydrazine

1.2 Other means of identification

Product number -
Other names N-phenyl-N-propagylhydrazine

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:61944-48-7 SDS

61944-48-7Downstream Products

61944-48-7Relevant academic research and scientific papers

Discovery of ectoparasiticidal hydrazonotrifluoromethanesulfonanilides

Ali, Abdelselam,Fisara, Petr,Freemont, Jamie A.,Kyi, Stella,Meyer, Adam G.,Riches, Andrew G.,Sargent, Roger M.,Sawutz, David G.,Turner, Kathleen A.,Winzenberg, Kevin N.,Yang, Qi

scheme or table, p. 649 - 652 (2010/06/12)

A series of hydrazonotrifluorosulfonanilide derivatives were synthesized and evaluated for in vitro activity against the ectoparasites Ctenocephalides felis and Rhipicephalus sanguineus. Some compounds with excellent activity against tick were identified.

Synthesis and reactions of the first allenyl azo compounds

Banert, Klaus,Hagedorn, Manfred,Schlott, Jana

, p. 360 - 361 (2007/10/03)

Several propargylhydrazines were prepared and then oxidized by manganese dioxide to generate short-lived 1,1-diazenes, which produced novel allenyl azo compounds (8) through [2,3] sigmatropic rearrangement. Isomerization of 8 or nucleophilic addition to the title compounds lead to hydrazones as well as pyrazole derivatives.

Synthesis of N-propargylphenelzine and analogues as neuroprotective agents

Ling, Lei,Urichuk, Liana J.,Sloley,Coutts, Ronald T.,Baker, Glen B.,Shan, Jacqueline J.,Pang, Peter K.T.

, p. 2715 - 2717 (2007/10/03)

A series of N1- and N2-propargylphenelzine derivatives and analogues (1-7) was synthesized. In addition to their activity as monoamine oxidase inhibitors, two of the compounds, N1- and N2-propargylphenelzines (3 and 6), were found to be potent at preventing DSP-4-induced noradrenaline (NA) depletion in mouse hippocampus, suggesting that they have neuroprotective properties.

Investigation of the Potential of Molybdenum(VI) Hydrazido(2-) Complexes as Sources of Nitrenium Ions: Cleavage of the N-N Bond and Incorporation of the β-Nitrogen Group into Solvent Molecules

Baum, Marc M.,Smith, Edward H.

, p. 2513 - 2520 (2007/10/02)

Photolyis or thermolysis of bis(N,N-dimethyldithiocarbamato)bismolybdenum(VI) complexes in 1,1,2,2-tetrachloroethane results predominantly in transfer of the hydrazido group to the solvent with formation of dichloroacetohydrazides.A small amount of the corresponding dichloroacetamides are produced by N-N cleavage and N(R)Ph transfer.In contrast, the latter process dominates the reaction of dichlorobis(N,N-dimethyldithiocarbamato)mono-molybdenum(VI) complexes with silver nitrate in alcohols occuring concomitantly with ring methoxylation and nitration and N-nitrosation.Neither transfer of N(R)Ph appears to involve free nitrenium ions.

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