71477-82-2 Usage
General Description
2,6-Diethylaniline·hydrochloride is a chemical compound that consists of 2,6-diethylaniline molecules combined with hydrochloric acid. It is often used as a reagent in organic synthesis and as a corrosion inhibitor in the petroleum industry. 2,6-Diethylaniline·hydrochloride is also utilized in the preparation of dyes and pharmaceuticals, as well as in the manufacturing of rubber chemicals and plasticizers. It has a wide range of applications in the chemical and pharmaceutical industries due to its stability, solubility, and ability to act as an intermediate in various organic reactions. Additionally, 2,6-Diethylaniline·hydrochloride is known for its low toxicity and is handled and used with appropriate safety measures.
Check Digit Verification of cas no
The CAS Registry Mumber 71477-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,7 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71477-82:
(7*7)+(6*1)+(5*4)+(4*7)+(3*7)+(2*8)+(1*2)=142
142 % 10 = 2
So 71477-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N.ClH/c1-3-8-6-5-7-9(4-2)10(8)11;/h5-7H,3-4,11H2,1-2H3;1H
71477-82-2Relevant articles and documents
Steric hindrance as a key factor on proton transfer in the σ-adduct forming reactions of o-substituted anilines with 1,3,5-trinitrobenzene in dimethylsulfoxide
Asghar, Basim H.
experimental part, p. 1191 - 1195 (2009/12/03)
Kinetic and equilibrium studies are reported of the reactions of 1,3,5-trinitrobenzene (TNB) with a series of o-substituted anilines in dimethyl sulfoxide (DMSO) in the presence of 1,4-diazabicyclo[2.2.2.]octane (DABCO). The pKa values in DMSO for the aniline derivatives were measured using the proton-transfer equilibrium with 2,4-dinitrophenol. Kinetic studies are compatible with a two-step process involving initial nucleophilic attack on TNB by amine to give a zwitterionic intermediate which may transfer an acidic proton to DABCO to yield the anionic product. The results indicate steric hindrance to proton transfer in reactions involving 2,6-disubstituted anilines.
