176641-35-3 Usage
Uses
Used in Pharmaceutical Research:
METHYL 6-METHOXY-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceutical compounds for the development of new drugs. Its unique structure and reactivity contribute to the exploration of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, METHYL 6-METHOXY-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLATE serves as a versatile building block for the creation of complex organic molecules. Its ester functionality allows for various chemical transformations, facilitating the synthesis of a wide range of organic compounds.
Used in Medicinal Chemistry:
METHYL 6-METHOXY-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLATE is utilized in the study of structure-activity relationships in medicinal chemistry. Its incorporation into different molecular frameworks helps researchers understand the impact of structural modifications on the biological activity of potential drug candidates.
Used in Drug Discovery:
In the drug discovery process, METHYL 6-METHOXY-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLATE is employed as a starting material or a scaffold for the design and optimization of new drug molecules. Its unique properties and reactivity enable the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research:
METHYL 6-METHOXY-1,2,3,4-TETRAHYDRO-QUINOLINE-2-CARBOXYLATE is a valuable tool in chemical research, where it is used to investigate various chemical reactions and mechanisms. Its reactivity and structural features provide insights into the fundamental aspects of organic chemistry and contribute to the advancement of the field.
Check Digit Verification of cas no
The CAS Registry Mumber 176641-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,6,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 176641-35:
(8*1)+(7*7)+(6*6)+(5*6)+(4*4)+(3*1)+(2*3)+(1*5)=153
153 % 10 = 3
So 176641-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO3/c1-15-9-4-6-10-8(7-9)3-5-11(13-10)12(14)16-2/h4,6-7,11,13H,3,5H2,1-2H3
176641-35-3Relevant academic research and scientific papers
Han, Caifang,Zhang,Feng, Xiangqing,Wang, Shoufeng,Du, Haifeng
, p. 1400 - 1403 (2018)
A metal-free hydrogenation of 2-quinolinecarboxylates has been realized by using 5 mol% of B(C6F5)3 as catalyst. A variety of tetrahydroquinolines were obtained in 57–99% yields. An attempt for the asymmetric hydrogenation with chiral boron Lewis acids generated from chiral dienes afforded very low ee's.
Enantioselective Synthesis of 2-Functionalized Tetrahydroquinolines through Biomimetic Reduction
Zhao, Zi-Biao,Wang, Jie,Zhu, Zhou-Hao,Chen, Mu-Wang,Zhou, Yong-Gui
supporting information, p. 9112 - 9117 (2021/11/24)
Biomimetic asymmetric reduction of 2-functionalized quinolines has been successfully developed with the chiral and regenerable NAD(P)H model CYNAM in the presence of transfer catalyst simple achiral phosphoric acids, providing the chiral 2-functionalized
Oxazoloquinolinone derivatives, their preparation and their therapeutic application as inhibitors of monoamine oxidase
-
, (2008/06/13)
3,3a,4,5-Tetrahydro-1H-oxazolo[3,4-a]quinolin-1-one derivatives of formula (I) STR1 in which: n is 0 or 1, R1 represents a hydrogen atom or an ethenyl, methyl, ethyl, phenyl, hydroxymethyl or methoxymethyl group, and (i) R2 is a meth
