91076-94-7 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL 3-AMINO-5-(4-CHLOROPHENYL)THIOPHE& is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a potential building block for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, ETHYL 3-AMINO-5-(4-CHLOROPHENYL)THIOPHE& is used as a precursor for the development of agrochemical products. Its chemical properties can be utilized to create new pesticides or herbicides with improved efficacy and selectivity.
It is important to handle and use ETHYL 3-AMINO-5-(4-CHLOROPHENYL)THIOPHE& with caution, as it may have harmful effects on human health and the environment if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 91076-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,7 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91076-94:
(7*9)+(6*1)+(5*0)+(4*7)+(3*6)+(2*9)+(1*4)=137
137 % 10 = 7
So 91076-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H12ClNO2S/c1-2-17-13(16)12-10(15)7-11(18-12)8-3-5-9(14)6-4-8/h3-7H,2,15H2,1H3
91076-94-7Relevant academic research and scientific papers
Synthesis of a series of novel thieno-and benzothieno[3,2-d]pyrimidin-4(3H) -ones
Abdillahi, Ismail,Kirsch, Gilbert
scheme or table, p. 1314 - 1318 (2011/05/19)
A series of novel thieno- and benzothieno[3,2-d]pyrimidin-4(3H)-ones is synthesised via condensation of 3-amino(benzo)thiophene-2-carboxylates with various lactams. Georg Thieme Verlag Stuttgart New York.
Synthesis of ethyl 3-amino-5-arylthiophene-2-carboxylates based on α-chlorocinnamonitriles
Shastin,Golubinskii,Lenkova,Balenkova,Nenaidenko
, p. 238 - 240 (2007/10/03)
A new procedure was developed for preparation of ethyl 3-amino-5- arylthiophene-2-carboxylates by the reaction of α-chlorocinnamonitriles and their analogs with ethyl mercaptoacetate for a wide range of substrates. The reaction products form in high yield
