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2-Methyl-3-oxanonane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18636-65-2

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18636-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18636-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,3 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18636-65:
(7*1)+(6*8)+(5*6)+(4*3)+(3*6)+(2*6)+(1*5)=132
132 % 10 = 2
So 18636-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-4-5-6-7-8-10-9(2)3/h9H,4-8H2,1-3H3

18636-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-propan-2-yloxyhexane

1.2 Other means of identification

Product number -
Other names Isopropylhexylaether

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:18636-65-2 SDS

18636-65-2Downstream Products

18636-65-2Relevant academic research and scientific papers

Uranyl(VI) Triflate as Catalyst for the Meerwein-Ponndorf-Verley Reaction

Kobylarski, Marie,Monsigny, Louis,Thuéry, Pierre,Berthet, Jean-Claude,Cantat, Thibault

supporting information, p. 16140 - 16148 (2021/11/01)

Catalytic transformation of oxygenated compounds is challenging in f-element chemistry due to the high oxophilicity of the f-block metals. We report here the first Meerwein-Ponndorf-Verley (MPV) reduction of carbonyl substrates with uranium-based catalysts, in particular from a series of uranyl(VI) compounds where [UO2(OTf)2] (1) displays the greatest efficiency (OTf = trifluoromethanesulfonate). [UO2(OTf)2] reduces a series of aromatic and aliphatic aldehydes and ketones into their corresponding alcohols with moderate to excellent yields, using iPrOH as a solvent and a reductant. The reaction proceeds under mild conditions (80 °C) with an optimized catalytic charge of 2.3 mol % and KOiPr as a cocatalyst. The reduction of aldehydes (1-10 h) is faster than that of ketones (>15 h). NMR investigations clearly evidence the formation of hemiacetal intermediates with aldehydes, while they are not formed with ketones.

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