13711-29-0 Usage
Uses
Used in Dye and Pigment Production:
2,3-Dichloro-5-methylaniline is utilized as a key intermediate in the synthesis of various dyes and pigments. Its chemical structure allows for the creation of a wide range of colorants, making it valuable in the production of colored products for different industries.
Used in Chemical Synthesis:
In the chemical industry, 2,3-Dichloro-5-methylaniline serves as a versatile building block for the synthesis of other organic compounds. Its reactivity and functional groups enable it to be a component in the production of various specialty chemicals and intermediates.
Safety Precautions:
Due to its toxic nature, 2,3-Dichloro-5-methylaniline can cause irritation to the skin, eyes, and respiratory system. It is crucial to handle and store this chemical with appropriate safety measures, including the use of personal protective equipment and proper containment to prevent exposure and potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 13711-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,1 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13711-29:
(7*1)+(6*3)+(5*7)+(4*1)+(3*1)+(2*2)+(1*9)=80
80 % 10 = 0
So 13711-29-0 is a valid CAS Registry Number.
13711-29-0Relevant academic research and scientific papers
3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands
Szymanska, Ewa,Pickering, Darryl S.,Nielsen, Birgitte,Johansen, Tommy N.
, p. 6390 - 6401 (2011/03/17)
On the basis of X-ray structures of ionotropic glutamate receptor constructs in complex with amino acid-based AMPA and kainate receptor antagonists, a series of rigid as well as flexible biaromatic alanine derivatives carrying selected hydrogen bond acceptors and donors have been synthesized in order to investigate the structural determinants for receptor selectivity between AMPA and the GluR5 subtype of kainate receptors. Compounds selective for either GluR5 or AMPA receptors were identified. One particular substituent position appeared to be of special importance for control of ligand selectivity. Using molecular modeling the observed structure-activity relationships at AMPA and GluR5 receptors were deduced.
Remarkable sensitivity to DNA base shape in the DNA polymerase active site
Sintim, Herman O.,Kool, Eric T.
, p. 1974 - 1979 (2007/10/03)
(Figure Presented) Shaping up: DNA polymerase I can distinguish easily and with high sensitivity between nucleobases that have the same size but differ in shape. The shape, altered through variation in the position of the halogen substituent(s), plays mor
