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3-(4-cyanophenoxy)benzoic acid is an organic compound with the chemical formula C14H9NO3. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 3-(4-cyanophenoxy)benzoic acid is characterized by its benzoic acid backbone, with a cyanophenoxy group attached at the 3-position. The presence of the cyano group (-CN) and the phenoxy group (C6H5O-) on the molecule gives it unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. The compound's structure allows for further functionalization and can be used as a building block in the synthesis of more complex molecules.

5128-55-2

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5128-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5128-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5128-55:
(6*5)+(5*1)+(4*2)+(3*8)+(2*5)+(1*5)=82
82 % 10 = 2
So 5128-55-2 is a valid CAS Registry Number.

5128-55-2SDS

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 (R)-Methyl 3-methyl-6-oxoheptanoate

1.2 Other means of identification

Product number -
Other names 3-Methyl-6-oxo-heptanoic acid methyl ester

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:5128-55-2 SDS

5128-55-2Downstream Products

5128-55-2Relevant academic research and scientific papers

Oxidation of 2-substituted cycloalkanones with cerium(IV) sulfate tetrahydrate in alcohols and acetic acid

He, Liangyou,Horiuchi, C. Akira

, p. 2515 - 2521 (2007/10/03)

The reaction of 2-substituted cycloalkanones with cerium(IV) sulfate tetrahydrate (CS) in alcohols and acetic acid gave the corresponding alkyl esters of oxo acids (80-96%) and oxo acids (78-96%), respectively, by oxidative cleavage of the C(R).C=O bond. In the case of 2-iodocycloalkanones in methanol, the dimethyl ester was obtained in good yield. A treatment of 5α-cholestan-3-one with CS in methanol produced 2-acetal 3-ester of 2,3-seco derivative in good yield. The effects of cerium(IV) and copper(II) salts are also discussed.

Oxidation of 2-alkylcycloalkanones with iodine-cerium(IV) salts in alcohols

He, Liangyou,Kanamori, Miyuki,Horiuchi, C. Akira

, p. 122 - 123 (2007/10/03)

The reaction of 2-alkylcycloalkanones with iodine-cerium(IV) salts in alcohols (methanol, ethanol, propan-1-ol or propan-2-ol) gave the respective oxo ester in 28-98% yields.

N-benzyl indol-3-yl butanoic acid derivatives as cyclooxygenase inhibitors

-

, (2008/06/13)

The invention encompasses the novel compound of Formula I useful in the treatment of cyclooxygenase-2 mediated diseases. STR1 The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula I.

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