27601-29-2 Usage
General Description
Tert-butyl (S)-[2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-2-oxo-1-[[4-(benzyloxy)phenyl]methyl]ethyl]carbamate is a complex chemical compound with a long and elaborate chemical structure. It is synthesized from a tert-butyl carbamate and contains a chiral center, denoted by the (S)- in its name, suggesting it has stereochemical specificity. The compound also includes a pyrrolidinyl group, a carbamate group, and a benzyloxyphenylmethyl group, indicating potential biological activity or pharmaceutical application. The specific properties, uses, and potential hazards of this chemical compound would require further analysis and evaluation.
Check Digit Verification of cas no
The CAS Registry Mumber 27601-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27601-29:
(7*2)+(6*7)+(5*6)+(4*0)+(3*1)+(2*2)+(1*9)=102
102 % 10 = 2
So 27601-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C25H28N2O7/c1-25(2,3)33-24(31)26-20(23(30)34-27-21(28)13-14-22(27)29)15-17-9-11-19(12-10-17)32-16-18-7-5-4-6-8-18/h4-12,20H,13-16H2,1-3H3,(H,26,31)/t20-/m0/s1
27601-29-2Relevant articles and documents
Antifungal amino acid derivative
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Paragraph 0138-0141, (2018/06/12)
PROBLEM TO BE SOLVED: To provide a new antifungal compound and an amino acid derivative with antifungal properties.SOLUTION: This invention relates to a compound represented by NHR-CHR-C(O)-R(I) or salt thereof, and an antifungal agent including the compound or salt thereof.
Novel Preparation of N-Protected Amino Acid Active Esters Using 1,2,2,2-Tetrachloroethyl Carbonates
Jaoudai, Mahmoud,Martinez, Jean,Castro, Bertrand
, p. 2364 - 2367 (2007/10/02)
1,2,2,2-Tetrachloroethyl chloroformate reacts with substituted phenols or N-hydroxy imides to yield crystalline and stable mixed aryl or oximido tetrachloroethyl carbonates.When allowed to react with an N-protected amino acid derivative, these compounds proved to be efficient for the syntheses of the corresponding active esters.A series of active esters including p-nitrophenol, trichlorophenol, pentafluorophenol, and N-hydroxysuccinimide derivatives were prepared by this new procedure.
