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104330-36-1

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104330-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104330-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104330-36:
(8*1)+(7*0)+(6*4)+(5*3)+(4*3)+(3*0)+(2*3)+(1*6)=71
71 % 10 = 1
So 104330-36-1 is a valid CAS Registry Number.

104330-36-1Relevant articles and documents

A highly efficient and convenient method for the direct conversion of alkyl THP ethers into the corresponding alkyl benzyl ethers

Suzuki, Takeshi,Ohashi, Kousaburo,Oriyama, Takeshi

, p. 1561 - 1563 (1999)

Direct conversion of alcohol tetrahydropyranyl (THP) ethers into the corresponding benzyl ethers can be conveniently performed by reaction with triethylsilane and benzaldehyde in the presence of a catalytic amount of trimethylsilyl trifluoromethanesulfona

Development of a Storable Triazinone-Based Reagent for O- p-Methoxybenzylation under Mild Heating Conditions

Fujita, Hikaru,Terasaki, Hiromitsu,Kakuyama, Satoshi,Hioki, Kazuhito,Kunishima, Munetaka

, (2019)

A new triazinone-based reagent for O-p-methoxybenzylation has been developed. In spite of its stability in solid form, this reagent converts a free alcohol into the corresponding p-methoxybenzyl ether with mild heating (50-60 °C) in a solution. High funct

p-Methylbenzyl 2,2,2-Trichloroacetimidate: Simple Preparation and Application to Alcohol Protection

Arai, Tomoki,Ikeuchi, Kazutada,Murasawa, Kentaro,Yamada, Hidetsohi

supporting information, p. 1034 - 1037 (2020/09/16)

A method for p-methylbenzyl (MBn) protection of alcohols by using MBn 2,2,2-trichloroacetimidate is described. The trichloroacetimidate can easily be prepared and isolated as a stable white powder without purification by silica gel chromatography. Catalytic use of zinc(II) triflate in diethyl ether activates the trichloroacetimidate to enable MBn protection of various alcohols.

Simple and rapid p-methoxybenzylation of hydroxy and amide groups at room temperature by NaOt-Bu and DMSO

Hamada, Shohei,Sugimoto, Koichi,Iida, Masashi,Furuta, Takumi

supporting information, (2019/11/13)

The p-methoxybenzylation of hydroxy and amide groups by p-methoxybenzyl chloride utilizing NaOt-Bu in DMSO is described. p-Methoxybenzylation of sterically hindered menthol using NaOt-Bu in DMSO proceeded faster than the commonly used methods which use Na

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