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1-(2,2,2-Trifluoroethyl)piperazine dihydrochloride is a chemical compound featuring a piperazine ring with a trifluoroethyl group attached to it. It is recognized for its potential pharmacological properties and is utilized as a building block in the synthesis of pharmaceutical compounds, particularly for the treatment of central nervous system disorders and other medical conditions. As a dihydrochloride salt, it exhibits high solubility in water, making it suitable for use in aqueous solutions for research and development.

13349-91-2

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13349-91-2 Usage

Uses

Used in Pharmaceutical Synthesis:
1-(2,2,2-Trifluoroethyl)piperazine dihydrochloride is used as a building block for the synthesis of various pharmaceutical compounds, leveraging its chemical structure to create potential drug candidates for the treatment of central nervous system disorders and other medical conditions.
Used in Research and Development:
In the field of research and development, 1-(2,2,2-Trifluoroethyl)piperazine dihydrochloride is used as a component in aqueous solutions due to its high solubility in water, facilitating the study of its pharmacological properties and potential applications in medicine.
Used in Neurology and Psychiatry:
1-(2,2,2-Trifluoroethyl)piperazine dihydrochloride is used in the field of neurology and psychiatry for its potential applications in treating central nervous system disorders. Its effects on the central nervous system are of particular interest, and ongoing research aims to explore its therapeutic potential in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 13349-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,4 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13349-91:
(7*1)+(6*3)+(5*3)+(4*4)+(3*9)+(2*9)+(1*1)=102
102 % 10 = 2
So 13349-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H11F3N2.2ClH/c7-6(8,9)5-11-3-1-10-2-4-11;;/h10H,1-5H2;2*1H

13349-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,2,2-Trifluoroethyl)piperazine dihydrochloride

1.2 Other means of identification

Product number -
Other names 1-(2,2,2-trifluoroethyl)piperazine,dihydrochloride

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:13349-91-2 SDS

13349-91-2Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLE COMPOUNDS AND METHODS OF USING THEM FOR TREATMENT OF HYPERPROLIFERATIVE DISEASES

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Paragraph 237, (2018/06/21)

Disclosed are compounds useful, for example, in methods of treating hyperproliferative disorders such as cancer, methods of arresting the cell cycle in cancer cells, methods of inhibiting glutathione synthesis in cancer cells, and associated compounds for

PHARMACEUTICAL COMPOUNDS

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Page/Page column 46-47, (2008/06/13)

Fused pyrimidines of formula (I); wherein A represents a thiophene or furan ring; n is 1 or 2; R1 is a group of formula (II); wherein m is 0 or 1; R30 is H or C1-C6 alkyl; R4 and R5 form, together with the N atom to which they are attached, a 5- or 6-membered saturated N-containing heterocyclic group which includes 0 or 1 additional heteroatoms selected from N, S and O, which may be fused to a benzene ring and which is unsubstituted or substituted; or one of R4 and R5 is alkyl and the other is a 5- or 6-membered saturated N-containing heterocyclic group as defined above or an alkyl group which is substituted by a 5- or 6-membered saturated N-containing heterocyclic group as defined above; R2 is selected from formula (a); wherein R6 and R7 form, together with the nitrogen atom to which they are attached, a morpholine, thiomorpholine, piperidine, piperazine, oxazepane or thiazepane group which is unsubstituted or substituted; and formula (b); wherein Y is a C2-C4 alkylene chain which contains, between constituent carbon atoms of the chain and/or at one or both ends of the chain, 1 or 2 heteroatoms selected from O, N and S, and which is unsubstituted or substituted; and R3 is an indazole group which is unsubstituted or substituted; and the pharmaceutically acceptable salt thereof have activity as inhibitors of P13K and may thus be used to treat diseases and disorders arising from abnormal cell growth, function or behaviour associated with P13 kinase such as cancer, immune disorders, cardiovascular disease, viral infection, inflammation, metabolism/endocrine disorders and neurological disorders. Processes for synthesizing the compounds are also described.

QUINAZOLINE DERIVATIVES AS SRC TYROSINE KINASE INHIBITORS

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Page 75, (2008/06/13)

The invention concerns quinazoline derivatives of Formula (I): (A chemical formula should be inserted here - please see paper copy enclosed herewith) wherein Z is an O, S, SO, SO2, N(R2) or C(R2)2 group wherein each R2 group is hydrogen or (1-8C) alkyl, m is 0, 1, 2 or 3, each R1 group is selected from halogeno, (1-8C) alkyl, (1-6C) alkoxy and any of the other meanings defined in the description, n is 0, 1, 2 or 3, and each R3 group is selected from halogeno, (1-8C) alkyl, (1-6C) alkoxy and any of the other meanings defined in the description, or pharmaceutically-acceptable salts thereof, processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an anti-invasive agent in the containment and/or treatment of solid tumour disease.

Substituted biphenyl isoxazole sulfonamides

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, (2008/06/13)

Compounds of the formula STR1 inhibit the activity of endothelin. The symbols are defined as follows: R1, R2, R3 and R4 are each directly bonded to a ring carbon and are each independently (a) hydrogen; (b) alkyl, alkenyl, alkynyl, alkoxy, cycloalkyl, cycloalkylalkyl, cycloalkenyl, cycloalkenylalkyl, aryl, aryloxy, aralkyl or aralkoxy, any of which may be substituted with Z1, Z2 and Z3 ; (c) halo; (d) hydroxyl; (e) cyano; (f) nitro; (g) --C(O)H or --C(O)R5 ; (h) --CO2 H or --CO2 R5 ; (i) --Z4 --NR6 R7 ; (j) --Z4 --N(R10)--Z5 --NR8 R9 ; or (k) R3 and R4 together may also be alkylene or alkenylene, either of which may be substituted with Z1, Z2 and Z3, completing a 4- to 8-membered saturated, unsaturated or aromatic ring together with the carbon atoms to which they are attached; and the remaining symbols are as defined in the specification.

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