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2-CYCLOHEXYL-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14087-90-2

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14087-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14087-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,8 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14087-90:
(7*1)+(6*4)+(5*0)+(4*8)+(3*7)+(2*9)+(1*0)=102
102 % 10 = 2
So 14087-90-2 is a valid CAS Registry Number.

14087-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclohexyl-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 2-cyclohexyl-3,4-dihydronaphthalen-1(2H)-one

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:14087-90-2 SDS

14087-90-2Relevant academic research and scientific papers

2-Aminotetralones: Novel inhibitors of MurA and MurZ

Dunsmore, Colin J.,Miller, Keith,Blake, Katy L.,Patching, Simon G.,Henderson, Peter J.F.,Garnett, James A.,Stubbings, William J.,Phillips, Simon E.V.,Palestrant, Deborah J.,Angeles, Joseph De Los,Leeds, Jennifer A.,Chopra, Ian,Fishwick, Colin W.G.

, p. 1730 - 1734 (2008/12/20)

Several 2-aminotetralones were identified as novel inhibitors of the bacterial enzymes MurA and MurZ. A number of these inhibitors demonstrated antibacterial activity against Staphylococcus aureus and Escherichia coli with MICs in the range 8-128 μg/ml. B

Catalytic cross-coupling of alkylzinc halides with α-chloroketones

Malosh, Chrysa F.,Ready, Joseph M.

, p. 10240 - 10241 (2007/10/03)

The cross-coupling of alkylzinc halides with α-chloroketones catalyzed by Cu(acac)2 is described. Using this method, primary and secondary alkyl groups are introduced adjacent to a ketone carbonyl under mild reaction conditions and in good yield. Cyclic, acyclic, aromatic, and aliphatic α-chloroketones are suitable substrates. Optically active α-chloroketones are converted to optically active products. The reaction was found to proceed stereospecifically with inversion of stereochemistry. The reaction is proposed to occur by direct substitution of the chloride with the alkyl group of an organocopper, -magnesium, or -zinc species. Copyright

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