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CAS

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898790-60-8

4-BROMOPHENYL CYCLOBUTYL KETONE is a chemical compound with the molecular formula C11H11BrO, featuring a cyclobutyl group and a bromophenyl group attached to the carbonyl carbon. It is a ketone commonly utilized in organic synthesis and research for the preparation of biologically active molecules and pharmaceuticals.

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  • 898790-60-8 Structure

  • Basic information

    1. Product Name: 4-BROMOPHENYL CYCLOBUTYL KETONE
    2. Synonyms: 4-BROMOPHENYL CYCLOBUTYL KETONE;UKRORGSYN-BB BBV-5118793
    3. CAS NO:898790-60-8
    4. Molecular Formula: C11H11BrO
    5. Molecular Weight: 239.11
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 898790-60-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 323.5°C at 760 mmHg
    3. Flash Point: 89.2°C
    4. Appearance: /
    5. Density: 1.456g/cm3
    6. Vapor Pressure: 0.000261mmHg at 25°C
    7. Refractive Index: 1.594
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-BROMOPHENYL CYCLOBUTYL KETONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-BROMOPHENYL CYCLOBUTYL KETONE(898790-60-8)
    12. EPA Substance Registry System: 4-BROMOPHENYL CYCLOBUTYL KETONE(898790-60-8)

  • 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: 898790-60-8(Hazardous Substances Data)

898790-60-8 Usage

Uses

Used in Organic Synthesis:
4-BROMOPHENYL CYCLOBUTYL KETONE is used as a building block for the synthesis of various biologically active molecules and pharmaceuticals, due to its unique structure and reactivity.
Used in Enzyme Inhibition Research:
4-BROMOPHENYL CYCLOBUTYL KETONE is used as a potential inhibitor of certain enzymatic reactions, making it a valuable compound in the study and development of new drugs.
Used in Pharmaceutical Development:
4-BROMOPHENYL CYCLOBUTYL KETONE is used as a starting material for the preparation of other functionalized aromatic compounds, which can be further utilized in the development of new pharmaceuticals through various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 898790-60-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,9 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 898790-60:
(8*8)+(7*9)+(6*8)+(5*7)+(4*9)+(3*0)+(2*6)+(1*0)=258
258 % 10 = 8
So 898790-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrO/c12-10-6-4-9(5-7-10)11(13)8-2-1-3-8/h4-8H,1-3H2

898790-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromophenyl)-cyclobutylmethanone

1.2 Other means of identification

Product number -
Other names (4-Bromophenyl)cyclobutyl-methanone

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:898790-60-8 SDS

898790-60-8Downstream Products

898790-60-8Relevant articles and documents

Synthesis and methemoglobinemia-inducing properties of analogues of para-aminopropiophenone designed as humane rodenticides

Rennison, David,Conole, Daniel,Tingle, Malcolm D.,Yang, Junpeng,Eason, Charles T.,Brimble, Margaret A.

supporting information, p. 6629 - 6635 (2014/01/06)

A number of structural analogues of the known toxicant para- aminopropiophenone (PAPP) have been prepared and evaluated for their capacity to induce methemoglobinemia - with a view to their possible application as humane pest control agents. It was found that an optimal lipophilicity for the formation of methemoglobin (metHb) in vitro existed for alkyl analogues of PAPP (aminophenones 1-20; compound 6 metHb% = 74.1 ± 2). Besides lipophilicity, this structural sub-class suggested there were certain structural requirements for activity, with both branched (10-16) and cyclic (17-20) alkyl analogues exhibiting inferior in vitro metHb induction. Of the four candidates (compounds 4, 6, 13 and 23) evaluated in vivo, 4 exhibited the greatest toxicity. In parallel, aminophenone bioisosteres, including oximes 30-32, sulfoxide 33, sulfone 34 and sulfonamides 35-36, were found to be inferior metHb inducers to lead ketone 4. Closer examination of Hammett substituent constants suggests that a particular combination of the field and resonance parameters may be significant with respect to the redox mechanisms behind PAPPs metHb toxicity.

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