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Ethanone, 1,2-diphenyl-, methylhydrazone is a chemical compound characterized by the presence of two benzene rings attached to a ketone group and a methylhydrazone substituent. It is known for its distinctive yellow color and is utilized in various applications due to its unique properties.

5172-07-6

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5172-07-6 Usage

Uses

Used in Organic Synthesis:
Ethanone, 1,2-diphenyl-, methylhydrazone serves as a reagent in organic synthesis, particularly for the formation of hydrazones. These hydrazones are crucial intermediates in a wide range of chemical reactions, making Ethanone, 1,2-diphenyl-, methylhydrazone an essential component in the synthesis of various organic compounds.
Used as a Dye or Indicator in Analytical Chemistry:
Due to its characteristic yellow color, Ethanone, 1,2-diphenyl-, methylhydrazone is often employed as a dye or indicator in analytical chemistry. Its color-changing properties can be utilized for detecting the presence of specific substances or monitoring chemical reactions.
Used in Medicine and Pharmacology:
Ethanone, 1,2-diphenyl-, methylhydrazone has been studied for its potential biological activity, suggesting that it may have applications in medicine and pharmacology. Further research is needed to explore its therapeutic potential and develop new drugs based on its chemical structure.

Check Digit Verification of cas no

The CAS Registry Mumber 5172-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5172-07:
(6*5)+(5*1)+(4*7)+(3*2)+(2*0)+(1*7)=76
76 % 10 = 6
So 5172-07-6 is a valid CAS Registry Number.

5172-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Desoxybenzoin-methylhydrazon

1.2 Other means of identification

Product number -
Other names -

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:5172-07-6 SDS

5172-07-6Relevant academic research and scientific papers

Benzothiadiphosphole as phosphorus donating reagent for a new route to 2H-1,2,3-diazaphosphole derivates

Baccolini,Orsolan,Mezzina

, p. 447 - 450 (2007/10/02)

Conjugated azoalkenes 2 react at reflux toluene with fused benzothiadiphosphole 1 (or 4) to give the diazaphosphole 3 in 25-52% yields. With this route it is possible to isolate the so far unknown 3a which is difficult to obtain in other reported conditions. The P atom involved in this cydoaddition is the one between the two S atoms.

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