527705-23-3 Usage
Derivative of benzoic acid
A modified version of benzoic acid It has a methylamino group attached to the benzene ring, giving it unique properties.
Usage as an intermediate
Pharmaceutical and agrochemical synthesis 2-[(Methylamino)methyl]benzoic acid can be used as a building block in the production of various pharmaceuticals and agrochemicals.
Potential as a corrosion inhibitor
Metal surface protection It has been studied for its ability to prevent or slow down the corrosion of metal surfaces.
Physical appearance
White crystalline solid The compound has a white, crystal-like appearance.
Solubility
Sparingly soluble in water, more soluble in organic solvents It does not dissolve well in water but has better solubility in certain organic solvents.
Hazardous if not handled properly
Safety precautions required Proper protective measures should be taken when handling this compound, as it may pose a risk to health or the environment if not managed correctly.
Check Digit Verification of cas no
The CAS Registry Mumber 527705-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,7,7,0 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 527705-23:
(8*5)+(7*2)+(6*7)+(5*7)+(4*0)+(3*5)+(2*2)+(1*3)=153
153 % 10 = 3
So 527705-23-3 is a valid CAS Registry Number.
527705-23-3Relevant articles and documents
Direct aerobic carbonylation of C(sp2)-H and C(sp3)-H bonds through Ni/Cu synergistic catalysis with DMF as the carbonyl source
Wu, Xuesong,Zhao, Yan,Ge, Haibo
supporting information, p. 4924 - 4927 (2015/05/05)
The direct carbonylation of aromatic sp2 and unactivated sp3 C-H bonds of amides was achieved via nickel/copper catalysis under atmospheric O2 with the assistance of a bidentate directing group. The sp2 C-H func
New protected protecting groups for the 5′-hydroxy group of deoxynucleosides by use of 2-(hydroxymethyl)- and 2-[(methylamino)methyl]benzoyl skeletons and oxidatively cleavable tritylthio and (4-methoxytrityl)thio groups
Seio, Kohji,Utagawa, Eri,Sekine, Mitsuo
, p. 2318 - 2333 (2007/10/03)
The new protecting groups 1a,b and 2a,b were developed for the 5′-OH group of deoxynucleosides by utilizing the unique characters of the sulfenate and sulfenamide linkage. These new protecting groups have a 2-(hydroxymethyl) benzoyl or 2-[(methylamino)met
