Welcome to LookChem.com Sign In|Join Free
  • or
2-methyl-benzoic acid; deprotonated form is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16887-74-4

Post Buying Request

16887-74-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

16887-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16887-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,8 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16887-74:
(7*1)+(6*6)+(5*8)+(4*8)+(3*7)+(2*7)+(1*4)=154
154 % 10 = 4
So 16887-74-4 is a valid CAS Registry Number.

16887-74-4Downstream Products

16887-74-4Relevant academic research and scientific papers

Concepts of sterically hindered resonance and buttressing effect: Gas-phase acidities of methyl-substituted benzoic acids and basicities of their methyl esters

Decouzon, Michèle,Ertl, Peter,Exner, Otto,Gal, Jean-Fran?ois,Maria, Pierre-Charles

, p. 12071 - 12078 (1993)

Two classical terms "Steric Hindrance to Resonance" and "Buttressing Effect" are revisited on the basis of the gas-phase acidities of nine methyl-substituted benzole acids and of the gas-phase basicities of their methyl esters, measured using FT- ICR spectrometry. By combining these data with published heats of formation of the neutrals and by using the principle of isodesmic reactions, relative enthalpies of formation were evaluated separately for the acid molecules, their anions (deprotonated), and their protonated cations (substituted by the protonated forms of the corresponding methyl esters). Energies of all species were also calculated at the semiempirical level (AMI). Substituent effects on the gas-phase acidity are similar to those on the acidity in water. All the methyl groups have a stabilizing polar effect, and o-methyl groups have a destabilizing steric effect, both effects increasing from the deprotonated forms to the acid molecules and then to the protonated forms. Separation of the two effects was attempted, assuming equal polar effects in the ortho and para positions. The results are internally consistent: their detailed analysis is in favor of a primary steric effect rather than a steric inhibition of resonance. The latter must be relatively weaker and operating only in 2,6-dimethyl derivatives, which are certainly nonplanar. In the literature this concept has been used too broadly, even for compounds for which the nonplanar conformation has not been proven. The concept of buttressing effect has been confirmed for methyl-substituted benzoic acids, but it is formulated more generally and more exactly. According to the new definition, it can be observed even for nonadjacent substituants.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 16887-74-4