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118652-88-3

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118652-88-3 Usage

General Description

3-Bromo-4-piperidinone hydrobromide is a chemical compound commonly used as a building block in the synthesis of pharmaceuticals and organic chemicals. It is a derivative of piperidinone and contains a bromine atom, making it reactive and useful for various chemical reactions. The hydrobromide salt form of this compound makes it more stable and easier to handle in laboratory settings. It is commonly used in the synthesis of antiviral and antibacterial medications, as well as in the production of agricultural chemicals. 3-Bromo-4-piperidinone hydrobromide is a versatile and important intermediate in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 118652-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 118652-88:
(8*1)+(7*1)+(6*8)+(5*6)+(4*5)+(3*2)+(2*8)+(1*8)=143
143 % 10 = 3
So 118652-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8BrNO.BrH/c6-4-3-7-2-1-5(4)8;/h4,7H,1-3H2;1H

118652-88-3SDS

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 3-bromopiperidin-4-one,hydrobromide

1.2 Other means of identification

Product number -
Other names 3-Bromopiperidin-4-one hydrobromide

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:118652-88-3 SDS

118652-88-3Relevant articles and documents

Small-molecule activity-based probe for monitoring ubiquitin C?terminal hydrolase L1 (UchL1) activity in live cells and zebrafish embryos

Kooij, Raymond,Liu, Sijia,Sapmaz, Aysegul,Xin, Bo-Tao,Janssen, George M.C.,van Veelen, Peter A.,Ovaa, Huib,ten Dijke, Peter,Geurink, Paul P.

, p. 16825 - 16841 (2020)

Many reagents have emerged to study the function of specific enzymes in vitro. On the other hand, target specific reagents are scarce or need improvement, allowing investigations of the function of individual enzymes in their native cellular context. Here we report the development of a target-selective fluorescent small-molecule activity-based DUB probe that is active in live cells and an in vivo animal model. The probe labels active ubiquitin carboxy-terminal hydrolase L1 (UCHL1), also known as neuron-specific protein PGP9.5 (PGP9.5) and Parkinson disease 5 (PARK5), a DUB active in neurons that constitutes 1 to 2% of the total brain protein. UCHL1 variants have been linked with neurodegenerative disorders Parkinson’s and Alzheimer’s diseases. In addition, high levels of UCHL1 also correlate often with cancer and especially metastasis. The function of UCHL1 activity or its role in cancer and neurodegenerative disease is poorly understood and few UCHL1-specific activity tools exist. We show that the reagents reported here are specific to UCHL1 over all other DUBs detectable by competitive activity-based protein profiling and by mass spectrometry. Our cell-penetrable probe, which contains a cyanimide reactive moiety, binds to the active-site cysteine residue of UCHL1 in an activity-dependent manner. Its use is demonstrated by the fluorescent labeling of active UCHL1 both in vitro and in live cells. We furthermore show that this probe can selectively and spatiotemporally report UCHL1 activity during the development of zebrafish embryos. Our results indicate that our probe has potential applications as a diagnostic tool for diseases with perturbed UCHL1 activity.

NOVEL COMPOUNDS

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Paragraph 0175; 0176, (2013/06/27)

This invention relates to compounds of formula I their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. A, B, X, R1, R2, R3 have meanings given in the description.

NOVEL COMPOUNDS

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Paragraph 0292; 0293; 0294, (2013/06/26)

This invention relates to compounds of formula I their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. A, B, X, R1, R2, R3 have meanings given in the description.

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