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Methanone, (4-hydroxy-1-phenyl-1H-pyrazol-3-yl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26502-72-7

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26502-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26502-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,0 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26502-72:
(7*2)+(6*6)+(5*5)+(4*0)+(3*2)+(2*7)+(1*2)=97
97 % 10 = 7
So 26502-72-7 is a valid CAS Registry Number.

26502-72-7SDS

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 (4-hydroxy-1-phenylpyrazol-3-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names (4-hydroxy-1-phenyl-1H-pyrazol-3-yl)-phenyl-methanone

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:26502-72-7 SDS

26502-72-7Downstream Products

26502-72-7Relevant academic research and scientific papers

THE SYNTHESIS OF 1H-PYRAZOL-4-OLS FROM 2-(2-ALKYLIDENEHYDRAZINO)ACETIC ACIDS

Pilling, Garry M.,Bell, Rebecca H.,Johnson, Robert E.

, p. 1341 - 1342 (2007/10/02)

A new general method for synthesizing 1H-pyrazol-4-ols by cyclizing 2-(2-alkylidenehydrazino)acetic acids with acetic anhydride in pyridine is reported.

Reactions of Glyoxals with Hydrazones: A New Route to 4-Hydroxypyrazoles

Begtrup, Mikael,Nytoft, Hans Peter

, p. 81 - 86 (2007/10/02)

N-Substituated hyrazones of aldehydes react with glyoxals under non-aqueous conditions to give N-substituted 4-hydroxypyrazoles; fourteen such products are described.In the presence of water, N-substituted 3-acyl-4-hydroxypyrazoles are produced from 2-oxoaldehyde hydrazones and glyoxals.It is shown that glyoxals combine in a 1:1 ratio with N-monosubstituted hydrazones to give 2-hydrazonoaldehydes as the kinetically controlled products.At room temperature or lower, these hydrazonoaldehydes rearrange to the more stable 2-oxoaldehyde hydrazones and react with glyoxals to give N-substituted 3-acyl-4-hydroxypyrazoles; sixteen such products are described.This synthesis, involving easily accessible starting materials, opens up a new, and for certain derivatives exclusive, route to 4-hydroxypyrazoles.

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