869996-05-4 Usage
Description
1-(2,2,2-Trifluoro-N-phenylethanimidate)-D-glucopyranuronic Acid Methyl Ester 2,3,4-Triacetate is a white powder compound with a unique chemical structure that features a trifluoro-N-phenylethanimidate group attached to a D-glucopyranuronic acid methyl ester with three acetate groups at the 2, 3, and 4 positions. This complex structure makes it a valuable compound for various applications in organic synthesis.
Uses
Used in Organic Synthesis:
1-(2,2,2-Trifluoro-N-phenylethanimidate)-D-glucopyranuronic Acid Methyl Ester 2,3,4-Triacetate is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for the formation of new chemical bonds and the synthesis of complex molecules, making it a valuable building block in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(2,2,2-Trifluoro-N-phenylethanimidate)-D-glucopyranuronic Acid Methyl Ester 2,3,4-Triacetate is used as a key intermediate in the synthesis of drug candidates. Its unique chemical properties enable the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Industry:
1-(2,2,2-Trifluoro-N-phenylethanimidate)-D-glucopyranuronic Acid Methyl Ester 2,3,4-Triacetate is also utilized in the agrochemical industry for the synthesis of new pesticides and herbicides. Its unique structure allows for the development of more effective and environmentally friendly crop protection agents.
Used in Specialty Chemicals:
In the specialty chemicals sector, 1-(2,2,2-Trifluoro-N-phenylethanimidate)-D-glucopyranuronic Acid Methyl Ester 2,3,4-Triacetate is employed as a versatile intermediate for the synthesis of various high-value chemicals. Its unique properties make it suitable for the development of advanced materials, dyes, and other specialty products.
Check Digit Verification of cas no
The CAS Registry Mumber 869996-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,9,9 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 869996-05:
(8*8)+(7*6)+(6*9)+(5*9)+(4*9)+(3*6)+(2*0)+(1*5)=264
264 % 10 = 4
So 869996-05-4 is a valid CAS Registry Number.
869996-05-4Relevant articles and documents
First O-glycosylation of hydroxamic acids
Thomas, Mickael,Gesson, Jean-Pierre,Papot, Sebastien
, p. 4262 - 4264 (2008/02/05)
(Chemical Equation Presented) The first O-glycosylation of hydroxamic acids is reported. This process involves the use of glycosyl N-phenyl trifluoroacetimidates as glycosyl donors in the presence TMSOTf and 4 A molecular sieves in dichloromethane. Under