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2-[(S)-4-isopropyl-4,5-dihydro-oxazol-2-yl]-6-methylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1104058-34-5

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1104058-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1104058-34-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,0,5 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1104058-34:
(9*1)+(8*1)+(7*0)+(6*4)+(5*0)+(4*5)+(3*8)+(2*3)+(1*4)=95
95 % 10 = 5
So 1104058-34-5 is a valid CAS Registry Number.

1104058-34-5Downstream Products

1104058-34-5Relevant academic research and scientific papers

A general and convenient route to oxazolyl ligands

Aspinall, Helen C.,Beckingham, Oliver,Farrar, Michael D.,Greeves, Nicholas,Thomas, Christopher D.

, p. 5120 - 5123 (2011/10/19)

A diverse range of chiral and achiral oxazolyl ligands, which have many applications including catalysis and luminescent devices, are synthesized simply in three steps from readily available and inexpensive phenol and amino alcohol starting materials. The method can be applied to ligands with electron-donating/-withdrawing and sterically demanding/undemanding substituents, and can conveniently be scaled up to >25 g of product.

Lewis base assisted Bronsted base catalysis: Bidentate phosphine oxides as activators and modulators of bronsted basic lanthanum-aryloxides

Morimoto, Hiroyuki,Yoshino, Tatsuhiko,Yukawa, Takafumi,Lu, Gang,Matsunaga, Shigeki,Shibasaki, Masakatsu

supporting information; experimental part, p. 9125 - 9129 (2009/02/08)

(Chemical Equation Presented) Dynamic Duo: A Lewis basic bidentate phosphine oxide was effective for activating and modulating the properties of Bronsted basic lanthanum aryl oxides. The Lewis base 1/lanthanum aryl oxide system was suitable for anti-selective Mannich-type reactions of trichloromethyl ketones (see scheme), affording unique building blocks for azetidine-2-carboxylic acids as well as β-amino acids.

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