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2-methyl-N'-phenylpropanehydrazide is a chemical compound with the molecular formula C10H14N2. It is a derivative of propanehydrazide, featuring a methyl group at the 2nd carbon and a phenyl group attached to the nitrogen atom. This organic compound is known for its potential applications in pharmaceuticals and as a chemical intermediate. It is characterized by its ability to form a hydrazone linkage, which is significant in the synthesis of various pharmaceuticals and agrochemicals. The compound's structure and reactivity make it a valuable component in the development of new drugs and chemical products.

5461-50-7

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5461-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5461-50-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5461-50:
(6*5)+(5*4)+(4*6)+(3*1)+(2*5)+(1*0)=87
87 % 10 = 7
So 5461-50-7 is a valid CAS Registry Number.

5461-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name isobutyric acid N'-phenyl-hydrazide

1.2 Other means of identification

Product number -
Other names Propanoic acid,2-methyl-,methyl ester

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:5461-50-7 SDS

5461-50-7Relevant academic research and scientific papers

Preparation of Complexes Bearing N-Alkylated, Anionic or Protic CAACs Through Oxidative Addition of 2-Halogenoindole Derivatives

Termühlen, Sebastian,Blumenberg, Jonas,Hepp, Alexander,Daniliuc, Constantin G.,Hahn, F. Ekkehardt

supporting information, p. 2599 - 2602 (2020/12/03)

CAAC precursors 2-chloro-3,3-dimethylindole 1 and 2-chloro-1-ethyl-3,3-dimethylindolium tetrafluoroborate 2BF4 have been prepared and oxidatively added to [M(PPh3)4] (M=Pd, Pt). Salt 2BF4 reacts with [Pd(PPh3)4] in toluene at 25 °C over 4 days to yield complex cis-[3]BF4 featuring an N-ethyl substituted CAAC, two cis-arranged phosphines and a chloro ligand. Compound trans-[3]BF4 was obtained from the same reaction at 80 °C over 1 day. Salt 2BF4 reacts with [Pt(PPh3)4] to give cis-[4]BF4. The neutral indole derivative 1 adds oxidatively to [Pt(PPh3)4] to give trans-[5] featuring a CAAC ligand with an unsubstituted ring-nitrogen atom. This nitrogen atom has been protonated with py?HBF4 to give trans-[6]BF4 bearing a protic CAAC ligand. The PdII complex trans-[7]BF4 bearing a protic CAAC ligand was obtained in a one-pot reaction from 1 and [Pd(PPh3)4] in the presence of py?HBF4.

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