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2,2-DIMETHYL-PIPERAZINE, a chemical compound with the molecular formula C6H14N2, is a cyclic amine characterized by the presence of two nitrogen atoms and two methyl groups attached to a six-membered ring. It is recognized for its versatile reactivity and ability to easily undergo substitution reactions, making it a valuable intermediate in organic synthesis.

84477-72-5

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84477-72-5 Usage

Uses

Used in Pharmaceutical Synthesis:
2,2-DIMETHYL-PIPERAZINE is utilized as a building block in the synthesis of pharmaceuticals, contributing to the development of various medicinal compounds due to its structural and reactive properties.
Used in Agrochemical Production:
In the agrochemical industry, 2,2-DIMETHYL-PIPERAZINE serves as a key component in the creation of compounds designed to protect crops and enhance agricultural productivity.
Used as a Curing Agent in Epoxy Resins:
2,2-DIMETHYL-PIPERAZINE is employed as a curing agent for epoxy resins, enhancing their properties and performance in various applications, including coatings, adhesives, and composite materials.
Used as a Corrosion Inhibitor in Metalworking Fluids:
2,2-DIMETHYL-PIPERAZINE is used as a corrosion inhibitor in metalworking fluids, helping to prevent the degradation of metal surfaces during manufacturing processes and extending the life of machinery and tools.
Used in Drug Delivery Systems:
2,2-DIMETHYL-PIPERAZINE has been evaluated for its potential as a drug delivery agent, particularly for targeting cancer cells and overcoming multidrug resistance, showcasing its utility in improving therapeutic outcomes in oncology.

Check Digit Verification of cas no

The CAS Registry Mumber 84477-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,7 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84477-72:
(7*8)+(6*4)+(5*4)+(4*7)+(3*7)+(2*7)+(1*2)=165
165 % 10 = 5
So 84477-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c1-6(2)5-7-3-4-8-6/h7-8H,3-5H2,1-2H3

84477-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dimethylpiperazine

1.2 Other means of identification

Product number -
Other names 2,2-dimethylpiperazine

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:84477-72-5 SDS

84477-72-5Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF 2,2-DIMETHYLPIPERAZINE

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Page/Page column 10-11, (2019/10/29)

This invention relates to a novel chemical process for the synthesis of 2,2-dimethylpiperazine and the further transformation of 2,2-dimethylpiperazine into ferf-butyl-3,3-dimethylpiperazine-l- carboxylate-hemi-DL-tartrate.

COMPOUNDS FOR REGULATING FAK AND/OR SRC PATHWAYS

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Page/Page column 113; 114, (2015/03/28)

The present application provides novel optionally substituted fused pyridine and pyrimidine bicyclic compounds and pharmaceutically acceptable salts thereof. Also provided are methods for preparing these compounds. These compounds are useful in co-regulating FAK and/or Src activity by administering a therapeutically effective amount of one or more of the compounds to a subject. By doing so, these compounds are effective in treating conditions associated with the dysregulation of the FAK and/or Src pathway. Advantageously, these compounds perform as dual FAK and/or Src inhibitors. A variety of conditions can be treated using these compounds and include diseases which are characterized by inflammation or abnormal cellular proliferation. In one embodiment, the disease is cancer.

COMPOUNDS, THEIR PHARMACEUTICAL COMPOSITIONS AND THEIR USES AS IDH1 MUTANTS INHIBITORS FOR TREATING CANCERS

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Page/Page column 115, (2013/02/28)

Provided are compounds of formula (I), wherein X, Y, Z, W, V, R2, R3 and m are defined as in the description. Their pharmaceutical compositions and their uses as IDH1 mutants inhibitors for treating cancers are also provided

Pharmaceutical compounds

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Page/Page column 90, (2008/06/13)

Compounds of Formulae Ia and Ib, and stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting lipid kinases including PI3K, and for treating disorders such as cancer mediated by lipid kinases. Methods of using compounds of Formula Ia and Ib for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

ALPHA-UNSUBSTITUTED ARYLMETHYL PIPERAZINE PYRAZOLO[1,5-A] PYRIMIDINE AMIDE DERIVATIVES

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Page/Page column 186, (2008/12/08)

Methods of preventing, treating or delaying the onset of HIV in a subject by administering to the subject novel pharmaceutically active arylmethyl pyrazolo[1,5-α ]pyrimidine amide derivatives, or pharmaceutical compositions containing the same are described. Additionally, compounds of novel pharmaceutically active arylmethyl piperazine pyrazolo[l,5-α]pyrimidine amide derivatives and their use for the manufacture of specific medicaments are described.

CRYSTALLINE BASE OF TRANS-1-((1R,3S)-6-CHLORO-3-PHENYLINDAN-1-YL)-3,3-DIMETHYLPIPERAZINE

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Page/Page column 15, (2008/06/13)

Crystalline base of compound trans-1-((1R,3S)-6-chloro-3-phenylindan-1-yl)-3,3-dimethylpiperazine, processes for the preparation of purified free base or salts of this compound, pharmaceutical compositions comprising the base and medical use thereof, incl

TARTRATE AND MALATE SALTS OF TRANS-1-((1R,3S)-6-CHLORO-3-PHENYLINDAN-1-YL)-3,3-DIMETHYLPIPERAZINE

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Page/Page column 14-15, (2008/06/13)

A tartrate and malate salt of trans-1-(6-chloro-3-phenylindan-1-yl)-3,3-dimethylpiperazine, in particular for medical use, pharmaceutical formulations thereof, including for treatment of schizophrenia or other diseases involving psychotic symptoms.

PROCESS FOR MAKING TRANS-1-((1R, 3S)-6-CHLORO-3-PHENYLINDAN-1-YL)-3, 3-DIMETHYLPIPERAZINE

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Page/Page column 20, (2008/06/13)

Described is a method for making the trans-1-((1R,3S)-6-chloro-3-phenylindan-1-yl)-3,3-dimethylpiperazine (formula I) and salts thereof and a similar method for making 4-((1R,3S)-6-chloro-3-phenylindan-1-yl)-1,2,2-trimethylpiperazine (formula IX) and salt

SUCCINATE AND MALONATE SALT OF TRANS-4-(IR,3S)-6-CHLORO-3-PHENYLINDAN-1-YL)-1,2,2-TRIMETHYLPIPERAZINE AND THE USE AS A MEDICAMENT

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Page/Page column 27-28, (2008/06/13)

4-((1R,3S)-6-Chloro-3-phenylindan-1-yl)-1,2,2-trimethylpiperazine hydrogen succinate or hadrogen malonat, pharmaceutical compositions containing these salts and the medical use thereof, including for the treatment of schizophrenia and other psychotic diso

1-PIPERAZINO-1,2-DIHYDROINDENE DERIVATIVES

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, (2008/06/13)

Trans isomers of 1-piperazino-1,2-dihydroindene compounds having formula (I), I wherein X and Y are hydrogen, halogen, trifluoromethyl, alkyl, alkylthio, trifluoromethylthio, alkoxy, hydroxy, alkylsulfonyl, amino, alkylamino, nitro or cyano; Ar is

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