104065-67-0 Usage
Uses
Used in Pharmaceutical Industry:
METHYL 3-METHOXY-2-PENTENOATE is used as an intermediate in the synthesis of prostaglandins for their role in regulating various physiological processes, such as inflammation, blood flow, and blood pressure. Prostaglandins are essential in the development of pharmaceuticals targeting these processes, making METHYL 3-METHOXY-2-PENTENOATE a vital component in the pharmaceutical industry.
Used in Chemical Synthesis:
METHYL 3-METHOXY-2-PENTENOATE is used as a building block in the synthesis of various organic compounds due to its reactive functional groups and unique structural features. Its versatility in chemical reactions allows it to be employed in the development of a wide range of products, from pharmaceuticals to specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 104065-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,6 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104065-67:
(8*1)+(7*0)+(6*4)+(5*0)+(4*6)+(3*5)+(2*6)+(1*7)=90
90 % 10 = 0
So 104065-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O3/c1-4-6(9-2)5-7(8)10-3/h5H,4H2,1-3H3/b6-5+
104065-67-0Relevant academic research and scientific papers
Magnesium(ii)-catalyzed asymmetric hetero-Diels-Alder reaction of Brassard's dienes with isatins
Zheng, Jianfeng,Lin, Lili,Kuang, Yulong,Zhao, Jiannan,Liu, Xiaohua,Feng, Xiaoming
supporting information, p. 994 - 996 (2014/01/06)
The first catalytic asymmetric hetero-Diels-Alder reaction of Brassard's dienes with isatins was realized using Mg(ii)/N,N′-dioxide complexes as catalysts, affording the corresponding chiral spirolactones bearing tetrasubstituted centers in up to 99% yield with up to 99% ee and >99:1 dr within 3 hours. In the mechanism, based on the operando IR experiments, a predominant Diels-Alder pathway was found in the reaction. A possible transition state model was also proposed. This journal is
Process for preparing 1,8-diethyl-1,3,4,9-tetrahydropyrano(3,4-b)-indole-1-acetic acid, etodolac
-
, (2008/06/13)
A process for preparing 1,8-diethyl-1,3,4,9-tetrahydro[3,4-b]-indole-1-acetic acid (etodolac) is disclosed. Etodolac is a useful antiinflammatory and analgesic agent.
