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1089174-47-9

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1089174-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1089174-47-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,9,1,7 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1089174-47:
(9*1)+(8*0)+(7*8)+(6*9)+(5*1)+(4*7)+(3*4)+(2*4)+(1*7)=179
179 % 10 = 9
So 1089174-47-9 is a valid CAS Registry Number.

1089174-47-9Downstream Products

1089174-47-9Relevant academic research and scientific papers

Friedel-Crafts acylation of aromatic compounds with carboxylic acids in the presence of P2O5/SiO2 under heterogeneous conditions

Zarei, Amin,Hajipour, Abdol R.,Khazdooz, Leila

, p. 6715 - 6719 (2008)

A convenient and efficient procedure for the Friedel-Crafts acylation of aromatic compounds with carboxylic acids in the presence of P2O5/SiO2 is described. Both aromatic and aliphatic carboxylic acids reacted easily to afford the corresponding aromatic ketones. The use of non-toxic and inexpensive materials, simple and clean work-up, short reaction times and good yields of the products are the advantages of this method.

Friedel-crafts acylation of arenes with carboxylic acids using polystyrene-supported aluminum triflate

Boroujeni, Kaveh Parvanak,Parvanak, Kamran

experimental part, p. 155 - 163 (2012/01/02)

Cross-linked polystyrene-supported aluminum triflate (Ps-Al(OTf) 3) has been shown to be a mild, efficient, and chemoselective heterogeneous Lewis acid catalyst for the acylation of aromatic compounds. The catalyst can be easily prepared from cheap starting materials, is stable (as a bench top catalyst) and is reusable.

Friedel-Crafts acylation of arenes with carboxylic acids using silica gel supported AlCl3

Parvanak Boroujeni, Kaveh

experimental part, p. 621 - 630 (2010/11/04)

Aromatic compounds react smoothly with carboxylic acids in the presence of silica gel supported aluminium trichloride to afford the corresponding ketones with high regioselectivity in high to excellent yields. The catalyst is stable (as a bench top catalyst) and can be easily recovered and reused without appreciable change in its efficiency. tuebitak.

Simple and efficient procedure for the friedel-crafts acylation of aromatic compounds with carboxylic acids in the presence of P2O5/AL2O3 under heterogeneous conditions

Hajipour, Abdol R.,Zarei, Amin,Khazdooz, Leila,Ruoho, Arnold E.

experimental part, p. 2702 - 2722 (2009/12/06)

An efficient and chemoselective method for the Friedel-Crafts acylation of aromatic compounds using P2O5/Al2O3 and carboxylic acids. Both aromatic and aliphatic carboxylic acids reacted easily to afford the corresponding aromatic ketones in good yields.

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