104085-30-5 Usage
Uses
Used in Organic Synthesis:
DIETHYL 2-([3-(BROMOMETHYL)-2-THIENYL]METHYLENE)MALONATE is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of a diverse array of organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, DIETHYL 2-([3-(BROMOMETHYL)-2-THIENYL]METHYLENE)MALONATE is used as a key intermediate in the development of new pharmaceutical drugs. Its unique structure allows for the creation of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Development:
DIETHYL 2-([3-(BROMOMETHYL)-2-THIENYL]METHYLENE)MALONATE also finds use in the agrochemical sector, where it is employed in the synthesis of new agrochemicals aimed at enhancing crop protection and productivity.
Used in Material Science:
DIETHYL 2-([3-(BROMOMETHYL)-2-THIENYL]METHYLENE)MALONATE is utilized in material science for the development of new materials with specific properties, such as improved stability or reactivity, which can be beneficial in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 104085-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,8 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104085-30:
(8*1)+(7*0)+(6*4)+(5*0)+(4*8)+(3*5)+(2*3)+(1*0)=85
85 % 10 = 5
So 104085-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H15BrO4S/c1-3-17-12(15)10(13(16)18-4-2)7-11-9(8-14)5-6-19-11/h5-7H,3-4,8H2,1-2H3
104085-30-5Relevant academic research and scientific papers
Lewis acid-mediated domino reaction of 3-bromomethylthiophenes with arenes/heteroarenes
Dhayalan, Vasudevan,Mohanakrishnan, Arasambattu K.
experimental part, p. 2149 - 2160 (2012/06/16)
Lewis acid-mediated domino reaction of 3-bromomethylthiophenes with various types of arenes and heteroarenes is reported.
Thienopyrroles: Synthesis, Diels-ALder Reaction, and Synthetic Utility
Sha, Chin-Kang,Tsou, Chiu-Peng
, p. 2446 - 2450 (2007/10/02)
5H-Thienopyrrole 1a and the N-substituted derivatives 1b-h and 11-13 were synthesized by the novel retro-malonate addition reaction.Thienopyrroles readily underwent the Diels-Alder reaction with reactive dienophiles, such as N-phenylmaleimid
Synthesis of 5H-Thienopyrrole
Sha, Chin-Kang,Tsou, Chiu-Peng
, p. 310 - 311 (2007/10/02)
5H-Thienopyrrole (4) was synthesized by a novel phosphineimine-alkylidenemalonate cyclization reaction.
