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1-Pentanol, 5-[(tetrahydro-2H-pyran-2-yl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76102-74-4

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76102-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76102-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,0 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76102-74:
(7*7)+(6*6)+(5*1)+(4*0)+(3*2)+(2*7)+(1*4)=114
114 % 10 = 4
So 76102-74-4 is a valid CAS Registry Number.

76102-74-4SDS

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 5-(oxan-2-yloxy)pentan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:76102-74-4 SDS

76102-74-4Relevant academic research and scientific papers

Phase-selective catalysis in emulsions stabilized by Janus silica-nanoparticles

Faria, Jimmy,Ruiz, M. Pilar,Resasco, Daniel E.

supporting information; experimental part, p. 2359 - 2364 (2011/02/21)

Metal-containing Janus particles are used as interfacial catalyst/emulsifiers that catalyze reactions in biphasic systems with controlled "phase selectivity", that is, conversion of the desired reaction on one side of the emulsion. The reaction may affect

Cerium(III) triflate versus cerium(III) chloride: Anion dependence of Lewis acid behavior in the deprotection of PMB ethers

Bartoli, Giuseppe,Dalpozzo, Renato,De Nino, Antonio,Maiuolo, Loredana,Nardi, Monica,Procopio, Antonio,Tagarelli, Antonio

, p. 2176 - 2180 (2007/10/03)

Cerium(III) triflate deprotects p-methoxybenzyl ethers of simple alcohols better than the cerium(III) chloride/sodium iodide system. It can be used in 1% M instead of equimolecular amounts, giving better yields. Aromatic alcohols rearrange, but the addition of a scavenger overcomes this drawback. Unfortunately, unsaturated alcohols are deprotected with decomposition, probably due to side electrophilic additions to double bonds. A comparison between the mechanisms of cerium triflate and cerium chloride is reported. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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