Home Impurity CS-T-93560

(3R,4R,5S)-4-(Acetylamino)-5-amino-3-(1-methylethoxy)-1-Cyclohexene-1-carboxylic Acid Ethyl Ester

Impurity CAT No. CS-T-93560 CAS No. 1052063-36-1
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Product Detail

(3R,4R,5S)-4-(Acetylamino)-5-amino-3-(1-methylethoxy)-1-Cyclohexene-1-carboxylic Acid Ethyl Ester

Impurity
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category Impurity
API Family --
Storage Refer MSDS for complete information.
Hazard Information Refer MSDS for complete information.

(3R,4R,5S)-4-(Acetylamino)-5-amino-3-(1-methylethoxy)-1-Cyclohexene-1-carboxylic Acid Ethyl Ester Product Information

(3R,4R,5S)-4-(Acetylamino)-5-amino-3-(1-methylethoxy)-1-Cyclohexene-1-carboxylic Acid Ethyl Ester is listed under Impurity. It is associated with and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-93560.

Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.

Technical Data

Product Name
(3R,4R,5S)-4-(Acetylamino)-5-amino-3-(1-methylethoxy)-1-Cyclohexene-1-carboxylic Acid Ethyl Ester
CAS No.
1052063-36-1
CAT No.
CS-T-93560
Molecular Formula
C₁₄H₂₄N₂O₄
Molecular Weight
284.35
Category
Storage Condition
Refer MSDS for complete information.
Hazard Compound
Refer MSDS for complete information.

Description

Overview
(3R,​4R,​5S)​-4-​(Acetylamino)​-​5-​amino-​3-​(1-​methylethoxy)​-1-​Cyclohexene-​1-​carboxylic Acid Ethyl Ester exhibits pharmacological activity regarding the inhibition of influenza A virus replication in combination with ribavirin and ozeltamivir.
Synonyms
Oseltamivir Impurity I;
Application Notes
(3R,​4R,​5S)​-4-​(Acetylamino)​-​5-​amino-​3-​(1-​methylethoxy)​-1-​Cyclohexene-​1-​carboxylic Acid Ethyl Ester exhibits pharmacological activity regarding the inhibition of influenza A virus replication in combination with ribavirin and ozeltamivir.
References
Konstantinova, I.; et al.: Russ. J. Bioorg. Chem, 39, 530 (2013)
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