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methyl 2-(piperazin-1-yl)ethanoate hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 196192-08-2 Structure
  • Basic information

    1. Product Name: methyl 2-(piperazin-1-yl)ethanoate hydrochloride
    2. Synonyms: methyl 2-(piperazin-1-yl)ethanoate hydrochloride
    3. CAS NO:196192-08-2
    4. Molecular Formula:
    5. Molecular Weight: 194.661
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 196192-08-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl 2-(piperazin-1-yl)ethanoate hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(piperazin-1-yl)ethanoate hydrochloride(196192-08-2)
    11. EPA Substance Registry System: methyl 2-(piperazin-1-yl)ethanoate hydrochloride(196192-08-2)
  • 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: 196192-08-2(Hazardous Substances Data)

196192-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 196192-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,1,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 196192-08:
(8*1)+(7*9)+(6*6)+(5*1)+(4*9)+(3*2)+(2*0)+(1*8)=162
162 % 10 = 2
So 196192-08-2 is a valid CAS Registry Number.

196192-08-2Downstream Products

196192-08-2Relevant articles and documents

Simplified procedure for general synthesis of monosubstituted piperazines-from a batch reaction vessel to a flow (microwave) reactor

?ev?ík, Richard,?imbera, Jan,Havránková, Eva,Něme?ková, Dana,Pazdera, Pavel

, (2020/05/25)

We reported a novel simplified synthetic procedure for the preparation of monosubstituted piperazine derivatives which can now be easily prepared in a one-pot-one-step way from a protonated piperazine with no need of introduction of a protecting group. Reactions, proceeding either at room or higher temperatures in common solvents, involve heterogeneous catalysis by metal ions supported on commercial polymeric resins. A general synthetic scheme was successfully applied to afford a wide range of monosubstituted piperazines. Furthermore, we picked up a set of piperazine derivatives and studied the possibilities of microwave acceleration of given synthetic reactions to make them even more efficient. Our research proceeded from a simple batch technique to the construction of a flow microwave reactor prototype and resulted in promising findings which are summarized and discussed in the article.

5-CHLORO-2-DIFLUOROMETHOXYPHENYL PYRAZOLOPYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF

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Paragraph 0760, (2015/12/05)

Compounds of Formula (00A) and methods of use as Janus kinase inhibitors are described herein.

NOVEL CONJUGATES, PREPARATION THEREOF, AND THERAPEUTIC USE THEREOF

-

, (2012/09/11)

Provided herein are cryptophycin conjugates and compositions containing them. Methods of making and using such compounds also are provided

NOVEL ADENINE COMPOUND

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Page/Page column 53, (2008/12/06)

An adenine compound or its pharmaceutically acceptable salt as a medicament as shown following formula (1): wherein R1 is optionally substituted alkyl group, etc., X is oxygen atom, etc., A is 4 to 8 membered optionally substituted saturated or unsaturated heterocyclic group containing 1 to 2 hetero atoms selected from 1 to 3 nitrogen atoms, 0 to 1 oxygen atom and 0 to 1 sulfur atom, L1 and L2 are independently straight or branched chain alkylene, or a single bond, R2 is optionally substituted alkyl group, etc.

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