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25292-25-5

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25292-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25292-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,9 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25292-25:
(7*2)+(6*5)+(5*2)+(4*9)+(3*2)+(2*2)+(1*5)=105
105 % 10 = 5
So 25292-25-5 is a valid CAS Registry Number.

25292-25-5SDS

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 2-benzyl-5-methylpyrazolidin-3-one

1.2 Other means of identification

Product number -
Other names 2-benzyl-5-methyl-pyrazolidin-3-one

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:25292-25-5 SDS

25292-25-5Downstream Products

25292-25-5Relevant articles and documents

Strategy to Prepare 3-Bromo- and 3-Chloropyrazoles

Fox, Richard J.,Schmidt, Michael A.,Eastgate, Martin D.

, p. 2830 - 2839 (2018/03/09)

A general strategy to prepare substituted 3-bromo- and 3-chloropyrazoles is described. The three-step method involves condensation of crotonates or β-chloro carboxylic acids with hydrazines, followed by halogenation and oxidation. Several condensation and oxidation protocols were developed to enable preparation of a wide variety of 3-halopyrazoles with good to excellent yields and regiocontrol.

Enantioselective conjugate addition of hydrazines to α,β- unsaturated imides. Synthesis of chiral pyrazolidinones

Sibi, Mukund P.,Soeta, Takahiro

, p. 4522 - 4523 (2007/10/03)

This manuscript describes a highly enantioselective conjugate hydrazine addition to α,β-unsaturated imides. The achiral template used has a significant impact on product enantioselectivity. Reactions at lower temperatures provide a protocol to add substit

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