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3-Pyrazolidinol, 2-benzoyl-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88418-55-7

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88418-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88418-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,1 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88418-55:
(7*8)+(6*8)+(5*4)+(4*1)+(3*8)+(2*5)+(1*5)=167
167 % 10 = 7
So 88418-55-7 is a valid CAS Registry Number.

88418-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-benzyl-5-hydroxypyrazolidin-1-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 1-benzoyl-2-benzyl-5-hydroxypyrazolidine

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:88418-55-7 SDS

88418-55-7Downstream Products

88418-55-7Relevant academic research and scientific papers

1-AROYL-2-BENZYL-5-HYDROXYPYRAZOLIDINES

Sviridova, L. A.,Afanas'eva, S. V.,Golubeva, G. A.,Torocheshnikov, V. N.,Terent'ev, P. B.,et al.

, p. 1001 - 1004 (2007/10/02)

The PMR spectral data show that 1-aroyl-2-benzyl-5-hydroxypyrazolidines are preferentially present in cyclic form in solution, while the proportion of the linear from increases to ca. 50percent in the gaseous phase, according to mass spectra.

SYNTHESIS OF 5-HYDROXY- AND 5-ACYLHYDRAZINOPYRAZOLIDINES BY THE REACTION OF &β-SUBSTITUTED HYDRAZIDES WITH &α,&β-UNSATURATED ALDEHYDES AND THEIR BIOLOGICAL ACTIVITY

Zelenin, K. N.,Dovgilevich, A. V.,Bezhan, I. P.,Golubeva, G. A.,Sviridova, L. A.,et al.

, p. 529 - 536 (2007/10/02)

The reaction of β-substituted hydrazides with alkenals (acrolein, methacrolein, crotonaldehyde, and cinnamaldehyde) serves as a method for the synthesis of the corresponding 1-acyl-5-hydroxypyrazolidines and, in a number of cases, 1-acyl-5-acylhydrazinopyrazolidines.Some of the 1-acyl-5-hydroxypyrazolidines obtained have antiphlogistic activity.

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