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1-Piperazineaceticacid,4-ethyl-,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 530098-58-9 Structure
  • Basic information

    1. Product Name: 1-Piperazineaceticacid,4-ethyl-,methylester(9CI)
    2. Synonyms: 1-Piperazineaceticacid,4-ethyl-,methylester(9CI);METHYL (4-ETHYLPIPERAZIN-1-YL)ACETATE
    3. CAS NO:530098-58-9
    4. Molecular Formula: C9H18N2O2
    5. Molecular Weight: 186.25
    6. EINECS: N/A
    7. Product Categories: PIPERIDINE
    8. Mol File: 530098-58-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Piperazineaceticacid,4-ethyl-,methylester(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Piperazineaceticacid,4-ethyl-,methylester(9CI)(530098-58-9)
    11. EPA Substance Registry System: 1-Piperazineaceticacid,4-ethyl-,methylester(9CI)(530098-58-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 530098-58-9(Hazardous Substances Data)

530098-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 530098-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,0,0,9 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 530098-58:
(8*5)+(7*3)+(6*0)+(5*0)+(4*9)+(3*8)+(2*5)+(1*8)=139
139 % 10 = 9
So 530098-58-9 is a valid CAS Registry Number.

530098-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(4-ethylpiperazin-1-yl)acetate

1.2 Other means of identification

Product number -
Other names methyl 4-ethylpiperazin-1-ylacetate

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:530098-58-9 SDS

530098-58-9Relevant articles and documents

NK1 and NK3 antagonists

-

Page/Page column 27, (2010/02/14)

The invention is to a compound exhibiting neurokinin inhibitory properties, a pharmaceutical composition comprising same and a method of treatment for neurokinin-mediated conditions.

Simons electrochemical fluorination of substituted homopiperazines(hexahydro-1,4-diazepines) and piperazines

Abe, Takashi,Baba, Hajime,Fukaya, Haruhiko,Tamura, Masanori,Sekiya, Akira

, p. 27 - 38 (2007/10/03)

Simons electrochemical fluorination (ECF) of 1,4-dimethyl-1,4-homopiperazine, methyl 4-ethylhomopiperazin-1-ylacetate and 1,4-bis(methoxycarbonylmethyl)-1,4-homopiperazine was studied. For comparison, ECF of three piperazines with a N-(methoxycarbonylmethyl) group(s) was also studied. ECF of 1,4-dimethyl-1,4-homopiperazine gave a low yield of corresponding perfluoro(1,4-dimethyl-1,4-homopiperazine) together with perfluoro(2,6-diaza-2,6-dimethylheptane) as the major product. Corresponding perfluoro(homopiperazines) with mono- and/or di-(fluorocarbonyldifluoromethyl) groups [-CF2C(O)F] at the 1- and/or 4-position were formed in low yields from methyl 4-ethylhomopiperazin-1-ylacetate and 1,4-bis(methoxycarbonylmethyl)-1,4-homopiperazine, respectively. These new seven-membered perfluoro(1,4-dialkyl-1,4-homopiperazines) were accompanied by the formation of mono- and/or di-basic linear perfluoroacid fluorides resulting from the C-C bond scission at the 2- and 3-positions of the ring. From mono- and/or di-N-(methoxycarbonylmethyl)-substituted piperazines, corresponding perfluoropeperazines having the acid fluoride group(s) were formed in low yields.

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