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Acetic acid, specifically the compound [3,5-bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-, is a derivative of acetic acid with a complex structure. This chemical features a cyclohexadienyl ring with a carbonyl group at position 4 and two tert-butyl groups (1,1-dimethylethyl) attached at positions 3 and 5. The presence of these bulky tert-butyl groups significantly influences the compound's physical and chemical properties, such as its reactivity, solubility, and stability. This specific acetic acid derivative may have unique applications in various fields, including pharmaceuticals, materials science, and organic synthesis, due to its distinct structural features and potential reactivity.

7019-94-5

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7019-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7019-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7019-94:
(6*7)+(5*0)+(4*1)+(3*9)+(2*9)+(1*4)=95
95 % 10 = 5
So 7019-94-5 is a valid CAS Registry Number.

7019-94-5Relevant academic research and scientific papers

Phosphine-Catalyzed Intermolecular Dienylation of Alkynoate with para-Quinone Methides

Song, Zefeng,Wang, Weijia,Liu, Zhixin,Lu, Yue,Wang, De

, p. 8590 - 8599 (2021/07/20)

An interesting remote I-C 1,6-Addition and an isomerization cascade reaction for phosphine-catalyzed activated alkynes have been disclosed. The products featuring a functional diene and a 1,1-diaryl methyl motif have been obtained in moderate to good yields (30-86%) by applying para-quinone methides (p-QMs) and I-substituted alkynoate with tributylphosphine (PnBu3) catalysis, along with high regioselectivity and stereoselectivity (dr > 20:1). The wide scope of compatible substrates (35 examples), such as indolyl, oxindolyl, ester, and cinnamyl, expand the utility of this methodology. A plausible mechanism and some applications of it have also been presented.

Palladium-Catalyzed Addition of Arylboronic Acids to para- Quinone Methides for Preparation of Diarylacetates

Zhuge, Ruijing,Wu, Liang,Quan, Mao,Butt, Nicholas,Yang, Guoqiang,Zhang, Wanbin

, p. 1028 - 1036 (2017/03/27)

A palladium-catalyzed addition of arylboronic acids to para-quinone methides has been developed. The catalytic system employing 4,4′-dimethoxy-2,2′-bipyridine (DMeO-BPy) as ligand and trifluoroethanol (TFE) as solvent provides diarylacetate products in high yields. A wide range of functionalized arylboronic acids can be used and the method tolerates some variation in the scope of the para-quinone methides. (Figure presented.).

Easy large scale syntheses of 2,6-di-t-butyl7-cyano-, 7-carboxy- and 7- methoxycarbonyl quinone methides

Nesvadba, Peter

, p. 2825 - 2832 (2007/10/03)

Easy large scale syntheses of 2,6-di-t-butyl-7-cyano-, 7-carboxy- and 7- methoxycarbonyl quinone methides 1-3 using cheap and readily available starting materials have been developed.

7-substituted quinone methides as inhibitors for unsaturated monomers

-

, (2008/06/13)

Ethylenically unsaturated monomers are protected from premature polymerization during manufacture and storage by the incorporation therein of an effective stabilizing amount of a 7-substituted quinone methide compound.

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