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Benzene, 1-[(1,1-dimethylethoxy)methyl]-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56636-80-7

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56636-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56636-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,3 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56636-80:
(7*5)+(6*6)+(5*6)+(4*3)+(3*6)+(2*8)+(1*0)=147
147 % 10 = 7
So 56636-80-7 is a valid CAS Registry Number.

56636-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-[(2-methylpropan-2-yl)oxymethyl]benzene

1.2 Other means of identification

Product number -
Other names 1-t-butoxymethyl-4-methoxybenzene

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:56636-80-7 SDS

56636-80-7Relevant academic research and scientific papers

Auto-Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones

Bakos, Mária,Gy?m?re, ádám,Domján, Attila,Soós, Tibor

supporting information, p. 5217 - 5221 (2017/04/27)

Herein we report that a single frustrated Lewis pair (FLP) catalyst can promote the reductive etherification of aldehydes and ketones. The reaction does not require an exogenous acid catalyst, but the combined action of FLP on H2, R-OH or H2O generates the required Br?nsted acid in a reversible, “turn on” manner. The method is not only a complementary metal-free reductive etherification, but also a niche procedure for ethers that would be either synthetically inconvenient or even intractable to access by alternative synthetic protocols.

Sulfated tungstate as hydroxyl group activator for preparation of benzyl, including p-methoxybenzyl ethers of alcohols and phenols

Katkar, Kamlesh V.,Veer, Sachin D.,Akamanchi, Krishnacharya G.

supporting information, p. 1893 - 1901 (2016/11/25)

Sulfated tungstate was found to be an effective heterogeneous and reusable catalyst for hydroxy group activation–mediated preparation of benzylic ethers including p-methoxybenzylic ethers of a wide range of alcohols and phenols under mild reaction conditions.

Gold(I)-catalyzed synthesis of unsymmetrical ethers using alcohols as alkylating reagents

Liu, Yongxiang,Wang, Xiaoyu,Wang, Yanshi,Du, Chuan,Shi, Hui,Jin, Shengfei,Jiang, Chongguo,Xiao, Jianyong,Cheng, Maosheng

, p. 1029 - 1036 (2015/03/30)

A microwave-irradiated alcohol-protecting strategy based on gold catalysis utilizing benzyl alcohol, tert-butyl alcohol and triphenylmethanol as alkylating reagents has been developed. This protecting strategy has wide functional group tolerance with satisfactory yields for the majority of the selected alcohols. The mechanism of this transformation was probed with oxygen-18 isotope labelled alcohols assisted by GC-MS techniques and chemical kinetic experiments. This strategy provides an efficient, straightforward and alternative approach to the preparation of benzyl, tert-butyl and trityl ethers in organic synthesis.

Simple and efficient method for the protection of hydroxyl groups as 4-methoxybenzyl ethers

Kasprzycka, Anna,Ptaszek-Budniok, Agata,Szeja, Wies?aw

supporting information, p. 2276 - 2284 (2014/07/07)

PMB ethers of alcohols are obtained in good yields and under mild conditions using the 4-methoxybenzyl N-allyl thiocarbamate and N-bromosuccinimide (NBS)/TfOH as the catalyst. The present method is very fast, simple, and efficient. Copyright

Proton-exchanged montmorillonite-mediated reactions of methoxybenzyl esters and ethers

Chen, Dongyin,Xu, Chang,Deng, Jie,Jiang, Chunhuan,Wen, Xiaoan,Kong, Lingyi,Zhang, Ji,Sun, Hongbin

, p. 1975 - 1983 (2014/03/21)

Proton-exchanged montmorillonite (H-mont) was found to be an eco-friendly and cost-effective catalyst for the generation of O-methylated quinone methides (QM) from the corresponding p or o-methoxybenzyl esters and ethers. Nucleophilic trapping of the O-methylated QM with arenes, alcohols, 1,3-dicarbonyl compounds, silyl enol ethers, and allylsilanes has been carried out, respectively, leading to eco-friendly benzylation reactions. Using this protocol, H-mont-mediated deprotection of PMB-protected esters and ethers have been realized for the first time. This work would pave the way for further exploration in O-alkylated QM that are of chemical and biological significance.

Competition of C-H and C-O fragmentation in substituted p-methoxybenzyl ether radical cations generated by photosensitized oxidation

Carlotti, Benedetta,Del Giacco, Tiziana,Elisei, Fausto

, p. 489 - 499 (2013/07/11)

Laser and steady-state photolysis, sensitized by 2,4,6-triphenylpyrylium tetrafluoroborate (TPP+BF4-), of 4-methoxybenzyl ethers [4-CH3O-C6H4CH(OR 1)R, 1a: R = H, R1 = CH3; 1b: R = H, R 1 = C(CH3)3; 1c: R = CH3, R 1 = C(CH3)3; 1d: R = 4-CH3O-C 6H4, R1 = CH3] was carried out in CH3CN in the presence of oxygen. In particular, steady-state irradiation of 1a, b and d produced benzylic alcohols (together with a small amount of acetamide for 1a and 1b) and the oxidation carbonyl compounds (esters and ketones); 4-methoxy-α-methylbenzyl alcohol was the only product observed with 1c. Time-resolved investigations of 1c and 1d gave evidence of the intermediate benzylic carbocation, coming from the ether radical cation formed within the laser pulse by an electron transfer process from the ether to the TPP+ excited state. These results suggested that, besides the deprotonation of the benzyl carbon, the cleavage of the C-OR1 bond is also operative in the reaction pathways of the ether radical cation. The comparison of these results with those obtained in the photolysis of 1c with the uncharged 9,10-dicyanoanthracene (DCA) upholds a particular behavior of TPP+BF4-, probably due to the specific electrostatic interactions of BF4- with the radical cation. This is also supported by quantum mechanical calculation results performed at the B3LYP/6-31G(d) level to obtain the charge and spin density distributions of radical cations, free and complexed with BF4 -.

A very practical and selective method for PMB protection of alcohols

Chavan, Subhash P.,Harale, Kishor R.

experimental part, p. 4683 - 4686 (2012/09/05)

A very simple, practical and efficient one-step heterogeneous protocol for the PMB protection of alcohols using Amberlyst-15 has been developed. The stability and hazard issues regarding PMBCl and PMBBr are totally avoided by directly using anisyl alcohol for the protection. Alcohols are protected in very good yields. The selective mono-PMB protection of diols as well as di-PMB protection of diols was achieved in good yields, along with the demonstration of recyclability of the catalyst.

Direct synthesis of unsymmetrical ethers from alcohols catalyzed by titanium cation-exchanged montmorillonite

Mitsudome, Takato,Matsuno, Tsuyoshi,Sueoka, Shoichiro,Mizugaki, Tomoo,Jitsukawa, Koichiro,Kaneda, Kiyotomi

supporting information; experimental part, p. 610 - 613 (2012/04/23)

Titanium-exchanged montmorillonite (Ti4+-mont) was found to act as an efficient heterogeneous catalyst for the etherification of a wide range of alcohols under mild reaction conditions. Ti4+-mont was reusable with retention of high efficiency and applicable to scale-up reaction conditions. The Royal Society of Chemistry 2012.

A simple and an efficient indium trichloride catalyzed benzyl etherification

Bhaskar,Solomon,Babu,Muralidharan,Perumal, Paramasivan T.

scheme or table, p. 795 - 801 (2011/01/04)

An efficient method has been developed for the synthesis of benzyl ethers of alkyl, allyl and propargyl alchols by simple, direct coupling of alcohols in the presence of catalytic amount of L1C13 under solvent-free condition.

Water compatible gold(III)-catalysed synthesis of unsymmetrical ethers from alcohols

Cuenca, Ana B.,Mancha, Gisela,Asensio, Gregorio,Medio-Simon, Mercedes

experimental part, p. 1518 - 1523 (2009/04/04)

An efficient and broad-scoped method for the preparation of unsymmetrical ethers from alcohols catalysed by the simplest and least expensive gold catalyst, NaAuCl4, is described for the first time. The procedure enables the etherification of benzylic and tertiary alcohols with moderate to good yields under mild conditions with low catalyst loading. Symmetrical ethers, the usual side products in the etherification of alcohols, were not detected in this case. The formation of the racemic ether from a chiral benzyl alcohol suggests the intermediacy of a carbocation, which has not previously been postulated for gold-catalysed reactions involving alcohols.

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