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129604-54-2

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129604-54-2 Usage

Uses

Used in Pharmaceutical Development:
1-(9H-FLUOREN-9-YL)PIPERAZINE is used as a building block for the development of new pharmaceuticals due to its unique chemical structure and potential therapeutic applications.
Used in Organic Synthesis:
1-(9H-FLUOREN-9-YL)PIPERAZINE is used as a key component in organic synthesis, contributing to the creation of various complex molecules and compounds.
Used in Cancer Treatment Research:
1-(9H-FLUOREN-9-YL)PIPERAZINE is used as a potential therapeutic agent in cancer treatment research, given its promising pharmacological properties and potential to target various diseases and disorders.
Used in Neurological Condition Treatment Research:
1-(9H-FLUOREN-9-YL)PIPERAZINE is used as a potential therapeutic agent in the treatment of neurological conditions, as it has shown promise in addressing various health issues in this area.
Used in Drug Development as a Ligand:
1-(9H-FLUOREN-9-YL)PIPERAZINE is used as a potential ligand in the development of new drugs and therapeutic agents, owing to its unique chemical properties and potential for medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 129604-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129604-54:
(8*1)+(7*2)+(6*9)+(5*6)+(4*0)+(3*4)+(2*5)+(1*4)=132
132 % 10 = 2
So 129604-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H18N2/c1-3-7-15-13(5-1)14-6-2-4-8-16(14)17(15)19-11-9-18-10-12-19/h1-8,17-18H,9-12H2

129604-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(9H-FLUOREN-9-YL)PIPERAZINE

1.2 Other means of identification

Product number -
Other names fluoren-9-ylpiperazine

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:129604-54-2 SDS

129604-54-2Relevant articles and documents

The second aryl piperazine compounds and their pharmaceutical use (by machine translation)

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, (2017/07/26)

The invention relates to the general formula I indicated by the two aryl piperazine compound, solvate, stereoisomer or a pharmaceutically acceptable salt thereof, pharmaceutical compositions containing them, and the compounds for the preparation for preventing or treating post-surgical pain, migraine, visceral pain, neuropathic pain such as the pain and analgesics such as by analgesic drug addiction and tolerance caused by the use of disease. (by machine translation)

PLASMINOGEN ACTIVATOR INHIBITOR-1 INHIBITOR

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Page/Page column 51, (2009/05/28)

The present invention relates to an inhibitor of plasminogen activator inhibitor-1. The present invention further relates to a pharmaceutical composition that has an inhibitory action on PAI-1 activity and is useful in the prevention and treatment of various diseases whose onset is associated with PAI-1 activity. Furthermore, the present invention relates to a novel compound having PAI-1 inhibitory activity represented by the following general formula (I), and a salt thereof. Each symbol is defined as those in the specification.

Amino acid derivative having anti-CCK activity

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, (2008/06/13)

A compound represented by the formula (1): STR1 wherein, m is an integer of 1 to 3; n is an integer 0 or 1; A represents CH or N atom, and forms together with the N atom bonded to the carbonyl group a piperidine ring or a piperazine ring; R1 independently represents a straight or branched chain alkyl group having 1 to 4 carbon atoms; a cycloalkyl group having 3 to 8 carbon atoms; a phenyl group, unsubstituted or substituted with a halogen atom or with an alkoxy group having 1 to 4 carbon atoms; or a pyridyl group; or two R1, together with the group >CH-- to which they bind, form a dibenzo cycloheptenyl group or a fluorenyl group; R2 represents a phenyl group substituted with a carboxyl or substituted carboxyl group; a pyridyl group substituted with a carboxyl or substituted carboxyl group, a pyrazyl group substituted with a carboxyl or substituted carboxyl group, an oxazolyl substituted with a carboxyl or substituted carboxyl group, a triazolyl substituted with one or two carboxyl or substituted carboxyl groups, or a phosphonopyridyl group; and R3 represents an indolyl group unsubstituted or substituted with a substituent selected from the group consisting of a halogen atom, a hydroxy group, an alkoxy group having 1 to 4 carbon atoms and methoxycarbonyl ethyl group and the pharmaceutically acceptable salts thereof.

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