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Tert-butyl (S)-[2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-2-oxo-1-[[4-(benzyloxy)phenyl]methyl]ethyl]carbamate is a complex organic chemical compound characterized by a long and intricate molecular structure. It is synthesized from a tert-butyl carbamate and features a chiral center, indicated by the (S)prefix, which denotes its stereochemical specificity. tert-butyl (S)-[2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-2-oxo-1-[[4-(benzyloxy)phenyl]methyl]ethyl]carbamate incorporates a pyrrolidinyl group, a carbamate group, and a benzyloxyphenylmethyl group, suggesting potential for biological activity or pharmaceutical applications. Further analysis and evaluation are necessary to determine its specific properties, uses, and potential hazards.

27601-29-2

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27601-29-2 Usage

Uses

Since the provided materials do not specify the uses of tert-butyl (S)-[2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-2-oxo-1-[[4-(benzyloxy)phenyl]methyl]ethyl]carbamate, it is not possible to list its applications based on the given information. However, given its complex structure and the presence of various functional groups, it may have potential applications in the pharmaceutical, chemical, or materials science industries. Further research and development would be required to explore and confirm its specific uses.

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

27601-29-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dioxopyrrolidin-1-yl) 2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(4-phenylmethoxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names Einecs 248-557-0

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:27601-29-2 SDS

27601-29-2Relevant academic research and scientific papers

Antifungal amino acid derivative

-

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.

β-lactam derivatives as enzyme inhibitors: Carboxy peptidyl derivatives of (S)-4-Oxoazetidine-2-carboxylate as peptidomimetics

Schneider, Martin,Otto, Hans-Hartwig

, p. 167 - 172 (2007/10/03)

4-Oxoazetidine-2-carboxylic acid, protected at the nitrogen by silyl groups, was coupled with amino acid and oligopeptide esters. Desilylation and deprotection of the amino acid residues yielded the free β-lactam peptides. Structure and properties were elucidated by spectroscopic methods and discussed. Some selected compounds Were tested as fibrinogen inhibitors and for thrombocyte aggregation. None of the compounds showed any activity up to a concentration of 10-5 Mol/1. Some other compounds exhibited a weak inhibitory activity against elastase (PPE).

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.

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