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(4-Hydroxyphenyl)trimethylammonium nitrate, also known as 4-(Trimethylammonio)phenol nitrate, is a quaternary ammonium compound with the chemical formula C9H14NO?NO3. It is a white crystalline solid that is soluble in water and exhibits strong electrophilic properties. (4-hydroxyphenyl)trimethylammonium nitrate is primarily used as a reagent in organic synthesis, particularly in the preparation of various phenolic derivatives and as a catalyst in certain chemical reactions. It is also known for its potential applications in the pharmaceutical industry and as a precursor to other chemical compounds. Due to its reactivity, it is important to handle this substance with care, following appropriate safety protocols.

92939-04-3

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92939-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92939-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,3 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92939-04:
(7*9)+(6*2)+(5*9)+(4*3)+(3*9)+(2*0)+(1*4)=163
163 % 10 = 3
So 92939-04-3 is a valid CAS Registry Number.

92939-04-3Downstream Products

92939-04-3Relevant academic research and scientific papers

Preparation and Characterization of Base-Sensitive Destructible Surfactants

Jaeger, David A.,Finley, C. Timothy,Walter, Mark R.,Martin, Craig A.

, p. 3956 - 3959 (1986)

Destructible surfactants 4-n-C12H25C6H4SO2CH2CH2OC6H4X-4 (1, X = N+Me3, NO3-; 2, X = SO3-, K+) were prepared, and their stability/lability characteristics in aqueous micellar solutions with respect to E1cB elimination to give 4-n-C12H25C6H4SO2CH=CH2 (7) and HOC6H4X-4 (8/9) were determined by 1H NMR.In 0.001 and 0.1 M DCl, both 1 and 2 were stable for 24 h at 75 deg C.In D2O alone at 25 deg C, 1 slowly decomposed, and 2 was stable.At 25 deg C, 1 decomposed completely within 10 min in 0.1 M NaHCO3, whereas 2 was more stable in 0.1 M K2CO3.The difference in reactivities for 1 and 2 was ascribed to a combination of electronic and micellar effects.Support for the latter was found in a comparison of 2's behavior with that of 4-MeC6H4SO2CH2CH2OC6H4SO3Na-4 (10).

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