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1728-46-7

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1728-46-7 Usage

Chemical Properties

clear colorless to light yellow-greenish liquid

Synthesis Reference(s)

Journal of the American Chemical Society, 107, p. 4679, 1985 DOI: 10.1021/ja00302a014Synthesis, p. 456, 1976 DOI: 10.1055/s-1976-24079

Check Digit Verification of cas no

The CAS Registry Mumber 1728-46-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1728-46:
(6*1)+(5*7)+(4*2)+(3*8)+(2*4)+(1*6)=87
87 % 10 = 7
So 1728-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-10(2,3)8-6-4-5-7-9(8)11/h8H,4-7H2,1-3H3/t8-/m1/s1

1728-46-7SDS

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 2-(tert-Butyl)cyclohexanone

1.2 Other means of identification

Product number -
Other names 2-TERT.-BUTYLCYCLOHEXANONE

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:1728-46-7 SDS

1728-46-7Relevant articles and documents

Solvent free ion exchange catalysis in the oxidation of organic compounds with sodium bromate

Shaabani, Ahmad,Lee, Donald G.

, p. 1255 - 1260 (2003)

The oxidation of organic compounds under solvent free ion exchange resin (IER) catalysis by sodium bromate has been studied at room temperature. Primary benzylic and secondary alcohols are converted to aldehydes and ketones and alkylarenes are oxidized to the corresponding α-ketones. The experimental procedure is simple and products are easily isolated in high yields at room temperature.

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

-

Paragraph 0094-0097; 0100-0104, (2021/05/29)

The invention belongs to the technical field of medicines, and discloses an aromatic compound hydrogenation and hydrodeoxygenation method under mild conditions and application of the method in hydrogenation and hydrodeoxygenation reactions of the aromatic compounds and related mixtures. Specifically, the method comprises the following steps: contacting the aromatic compound or a mixture containing the aromatic compound with a catalyst and hydrogen with proper pressure in a solvent under a proper temperature condition, and reacting the hydrogen, the solvent and the aromatic compound under the action of the catalyst to obtain a corresponding hydrogenation product or/and a hydrodeoxygenation product without an oxygen-containing substituent group. The invention also discloses specific implementation conditions of the method and an aromatic compound structure type applicable to the method. The hydrogenation and hydrodeoxygenation reaction method used in the invention has the advantages of mild reaction conditions, high hydrodeoxygenation efficiency, wide substrate applicability, convenient post-treatment, and good laboratory and industrial application prospects.

Selective phenol hydrogenation under mild condition over Pd catalysts supported on Al2O3 and SiO2

Li, Xinzheng,Cheng, Ling,Wang, Xingyi

, p. 1249 - 1262 (2019/02/24)

Cyclohexanone (CHONE) is the key intermediate in the manufacture of nylon-6 and nylon-66. Selective hydrogenation of phenol into CHONE was investigated over Pd/SiO2 and Pd/Al2O3. The results show that the yield of CHONE reaches 98% or more over Pd/Al2O3 and Pd/SiO2 at 333?K under atmospheric pressure in cyclohexane solvent. High activity of Pd/Al2O3 is promoted by Lewis acidity, and phenol can be converted 100% within 300?min. The hydrogenation of CHONE occurs until the conversion of phenol approaches completion. Pd/SiO2 with smaller Pd nano-particles presents higher selectivity. For polar solvent, such as ethanol and dichloromethane, the activity of Pd catalysts decreases greatly. Auxiliary experiments verify that phenol adsorbs on Pd catalysts via the formation of π–c with an aromatic ring. Increased hydrogen pressure not only promotes significantly the rates of hydrogenation, but also increases the selectivity for CHONE, especially over Pd/SiO2-1 catalyst.

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