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88547-15-3

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88547-15-3 Usage

Chemical structure

heterocyclic organic compound with a piperazine ring

Physical appearance

white to off-white crystalline solid

Uses

building block in the synthesis of pharmaceuticals and agrochemicals, valuable intermediate for the production of various other chemical compounds

Properties

may pose health and environmental hazards, handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 88547-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88547-15:
(7*8)+(6*8)+(5*5)+(4*4)+(3*7)+(2*1)+(1*5)=173
173 % 10 = 3
So 88547-15-3 is a valid CAS Registry Number.

88547-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2,5-diketopiperazine

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:88547-15-3 SDS

88547-15-3Relevant articles and documents

EPIDITHIODIOXOPIPERAZINE COMPOUND OR ITS DERIVATIVES, AND THE USE THEREOF

-

Paragraph 387; 392-394, (2014/12/12)

The present invention relates to an epidithiodioxopiperazine derivative represented by the Chemical Formula 1 or its reduced derivative; a method for preparing a compound represented by Chemical Formula 1 having improved intracellular permeability and mim

Comparative study of synthetic approaches to 1- arylmethylenepyrazino[2,1-b]quinazoline-3,6-diones

Cledera, Pilar,Avendano, Carmen,Menendez, J. Carlos

, p. 12349 - 12360 (2007/10/03)

The transformation of 3-arylmethylenepiperazine-2,5-diones (1) into 1- arylmethylene-2,4-dihydro-1H-pyrazino[2,1-b]quinazoline-3,6-diones (2) was studied. Four synthetic methods were compared, namely direct condensation with the product of the reaction be

Synthesis, Antibacterial Activities, and Pharmacological Properties of Enantiomers of Temafloxacin Hydrochloride

Chu, Daniel T. W.,Nordeen, Carl W.,Hardy, Dwight J.,Swanson, Robert N.,Giardina, William J.,et al.

, p. 168 - 174 (2007/10/02)

Temafloxacin hydrochloride is a potent member of the 4-pyridone-3-carboxylic acid class of antibacterial agents and is currently under clinical development as a broad-spectrum antimicrobial agent.It is a racemate having a chiral center at the C3 of the 7-piperazin-1-yl group.The two enantiomers were synthesized and tested for their antibacterial activities.Although no difference in in vitro antibacterial activities was observed, a minor difference in in vivo antibacterial activities was observed.However, they both exhibited similar pharmacological profiles.

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