51114-26-2 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL [(CHLOROACETYL)(PHENYL)AMINO]ACETATE is used as an intermediate in the synthesis of various drugs for its ability to combine with other chemical groups to form new compounds with therapeutic properties.
Used in Agricultural Chemicals Production:
ETHYL [(CHLOROACETYL)(PHENYL)AMINO]ACETATE is used in the production of agricultural chemicals for its ability to contribute to the formation of compounds that can help control pests and diseases in crops.
Used in Dyes Production:
ETHYL [(CHLOROACETYL)(PHENYL)AMINO]ACETATE is used in the production of dyes for its ability to contribute to the formation of colorants used in various industries, such as textiles and plastics.
Check Digit Verification of cas no
The CAS Registry Mumber 51114-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,1 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51114-26:
(7*5)+(6*1)+(5*1)+(4*1)+(3*4)+(2*2)+(1*6)=72
72 % 10 = 2
So 51114-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H14ClNO3/c1-2-17-12(16)9-14(11(15)8-13)10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
51114-26-2Relevant academic research and scientific papers
GLYCINE B ANTAGONISTS
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Page/Page column 57, (2010/12/29)
The invention relates to naphthalene derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are glycine B antagonists and are therefore useful for the control and prevention of various disorders, including neurological disorders.
Intramolecular aza-wittig reaction: A new efficient tool for the construction of piperazine 2,5-dione derivatives
Majumdar,Ray, Krishanu,Ganai, Sintu
supporting information; experimental part, p. 2122 - 2124 (2010/10/03)
A new efficient approach for the synthesis of unsymmetricaly substituted piperazine 2,5-dione derivatives is described by using intramolecular aza-Wittig reaction as the key step. The reaction conditions are very simple, offer easy isolation, and excellen
