52659-18-4 Usage
Uses
Used in Pharmaceutical Industry:
METHYL-3-N-ACETYLAMINO PHTHALATE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex drug molecules. Its unique structure allows it to be a key component in developing new medications.
Used in Agrochemical Industry:
In the agrochemical sector, METHYL-3-N-ACETYLAMINO PHTHALATE is employed as an intermediate in the production of various agrochemicals. Its role in creating essential compounds aids in enhancing crop protection and agricultural productivity.
Used in Dye Industry:
METHYL-3-N-ACETYLAMINO PHTHALATE is utilized as an intermediate in the manufacturing of dyes due to its capacity to be incorporated into the structures of diverse colorants. This contributes to the development of a wide range of dyes used in various applications.
Safety Note:
It is crucial to handle METHYL-3-N-ACETYLAMINO PHTHALATE with care and adhere to proper safety protocols to minimize potential health hazards associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 52659-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,5 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52659-18:
(7*5)+(6*2)+(5*6)+(4*5)+(3*9)+(2*1)+(1*8)=134
134 % 10 = 4
So 52659-18-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO5/c1-7(14)13-9-6-4-5-8(11(15)17-2)10(9)12(16)18-3/h4-6H,1-3H3,(H,13,14)
52659-18-4Relevant academic research and scientific papers
Discovery of indenopyrazoles as EGFR and VEGFR-2 tyrosine kinase inhibitors by in silico high-throughput screening
Usui, Taikou,Ban, Hyun Seung,Kawada, Junpei,Hirokawa, Takatsugu,Nakamura, Hiroyuki
, p. 285 - 288 (2008/09/17)
A series of indenopyrazoles 8 and 9 were designed and synthesized as EGFR tyrosine kinase inhibitors by in silico high-throughput screening. Compounds 8b and 8d showed significant inhibition of A431 cell growth (GI50 = 0.062 and 0.057 μM, respectively). Compounds 8b and 9a showed inhibitory activity toward both EGFR and VEGFR-2 (KDR) tyrosine kinases, whereas 8d inhibited VEGFR-2 tyrosine kinase, exclusively.
