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Benzenemethanol, a-methyl-4-(1-methylpropyl)-, also known as 4-isobutyl-α-methylbenzyl alcohol or 4-isobutyl-α-methylbenzenemethanol, is an organic compound with the chemical formula C12H18O. It is a colorless liquid with a molecular weight of 178.27 g/mol. Benzenemethanol, a-methyl-4-(1-methylpropyl)- is characterized by a benzyl alcohol structure, where the benzene ring is substituted with a methyl group at the α-position and an isobutyl group at the 4-position. It is used as a fragrance ingredient and a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is insoluble in water but soluble in organic solvents, and it has a specific gravity of 0.94 and a boiling point of 255°C.

7641-91-0

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7641-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7641-91-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,4 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7641-91:
(6*7)+(5*6)+(4*4)+(3*1)+(2*9)+(1*1)=110
110 % 10 = 0
So 7641-91-0 is a valid CAS Registry Number.

7641-91-0Downstream Products

7641-91-0Relevant academic research and scientific papers

Achiral and chiral NNN-pincer nickel complexes with oxazolinyl backbones: application in transfer hydrogenation of ketones

Jagtap, Rahul A.,Ankade, Shidheshwar B.,Gonnade, Rajesh G.,Punji, Benudhar

, p. 11927 - 11936 (2021/07/17)

We describe the synthesis of new NNN-oxazolinyl-pincer nickel complexes and their application in the transfer hydrogenation of ketones. Achiral NNN-ligands, R′2-oxazolinyl-2-C6H4-NH-C(O)CH2NEt2[(

FLASH VACUUM THERMOLYSIS OF DISPIROALKADIENES

Kraakmann, P. A.,Nibbering, E. T. J.,Wolf, W. H. de,Bickelhaupt, F.

, p. 5109 - 5124 (2007/10/02)

The Flash Vacuum Thermolysis (FVT) of dispirotetradeca -4,13-diene (7a). dispirotrideca-4,12-diene (7b) and dispirodeca-4,9-diene (7e) at 500-750 deg C is reported.The complicated reaction mixture from 7a and 7b (Scheme 3) included at lower temperatures vinylspiroalkadienes 9, ethylidenespiroalkadiene 10b, β-ethylcycloalkabenzenes 11, while at higher temperatures, p-n-alkyl-(5) and p-sec-alkylstyrenes 14 and p-divinylbenzene (15) dominated.Product formation is explained by invoking diradicals 8,6 and 12 as well as the cyclophanes 1 and 13 as intermediates.For 7e, the product mixture was less complicated and consisted of p-ethylstyrene (5e), 15 and, unexpectedly,p-isopropylstyrene (14e) which contains one carbon more than the starting material.The analysis and interpretation of product formation largely confirms previously suggested reaction pathways and furnishes further interesting details.However, new and unexpected features are also encountered, especially in the fragmentations of 1 and 13 which may stimulate future investigations on the thermal behaviour of these relatively simple hydrocarbons.

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