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3,5-diphenyl-1H-pyrazol-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17953-06-9

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17953-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17953-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,5 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17953-06:
(7*1)+(6*7)+(5*9)+(4*5)+(3*3)+(2*0)+(1*6)=129
129 % 10 = 9
So 17953-06-9 is a valid CAS Registry Number.

17953-06-9SDS

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 3,5-diphenyl-1H-pyrazol-4-ol

1.2 Other means of identification

Product number -
Other names 3,5-Diphenyl-4-hydroxy-pyrazol

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:17953-06-9 SDS

17953-06-9Relevant academic research and scientific papers

A multi-substituted 4 - hydroxy pyrazole derivatives of the preparation method

-

Paragraph 0025; 0028; 0029, (2017/08/25)

The invention provides a preparation method of a multi-substituted 4-hydroxypyrazole derivative. An alkenyl azide derivative and a hydrazine compound which are chemically synthesized easily are generated under the condition of room temperature. The provid

Synthesis of polysubstituted 4-aminopyrazoles and 4-hydroxypyrazoles from vinyl azides and hydrazines

Huang, Wei,Liu, Shen,Chen, Binhui,Guo, Xiao,Yu, Yongping

, p. 32740 - 32743 (2015/04/27)

A simple and direct synthesis of polysubstituted 4-aminopyrazoles and 4-hydroxypyrazoles from vinyl azides and hydrazines was developed. The present reactions were performed under mild conditions in moderate to excellent yields. A possible mechanism is al

Synthesis and biological properties of 2-pyrrolidinoethoxy derivatives of 3,5-diarylpyrazoles and 2-pyrazolines

Sangwan, Naresh K.,Verma, Braham S.,Dhindsa, Kuldip Singh

, p. 508 - 512 (2007/10/02)

Cyclization of 2'-or 4'-hydroxy-4-methoxychalkone (1,2) with hydrazine hydrate in refluxing formic or acetic acid gives 1-acyl-5-aryl-3-(2-or 4-hydroxyphenyl)-2-pyrazolines (3-6).Alkylation of 1-6 and 4-hydroxy-3,5-diphenylpyrazole (17) with N-(2-chloroet

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