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2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (1R)-4-(diphenylaMino)-1-Methyl-4-oxo-2-butyn-1-yl ester, (2E)is a complex organic compound that features a 2-propenoic acid backbone, a nitro-cyclohexene moiety, and a diphenylamino group. This ester is characterized by its unique molecular structure, which includes a butyn-1-yl ester group. Although its specific properties and potential applications are not fully understood, the presence of these functional groups suggests that it may have a range of chemical and biological uses.

899809-60-0

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899809-60-0 Usage

Uses

Used in Chemical Synthesis:
2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (1R)-4-(diphenylaMino)-1-Methyl-4-oxo-2-butyn-1-yl ester, (2E)is used as a chemical intermediate in the synthesis of various organic compounds. Its unique structure, which includes a nitro-cyclohexene moiety and a diphenylamino group, makes it a versatile building block for the development of new molecules with potential applications in various industries.
Used in Pharmaceutical Research:
2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (1R)-4-(diphenylaMino)-1-Methyl-4-oxo-2-butyn-1-yl ester, (2E)is used as a starting material in the development of new pharmaceutical compounds. The presence of the nitro-cyclohexene and diphenylamino groups may provide opportunities for the design of novel drugs with unique mechanisms of action. Further research is needed to explore its potential as a therapeutic agent.
Used in Material Science:
2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (1R)-4-(diphenylaMino)-1-Methyl-4-oxo-2-butyn-1-yl ester, (2E)may be used in the development of new materials with specific properties. Its molecular structure, which includes a butyn-1-yl ester group, could be exploited to create materials with unique mechanical, electrical, or optical properties. Further investigation is required to determine its potential applications in this field.
Used in Agrochemical Development:
2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (1R)-4-(diphenylaMino)-1-Methyl-4-oxo-2-butyn-1-yl ester, (2E)may have potential applications in the agrochemical industry as a precursor for the synthesis of new pesticides or herbicides. Its unique structure could be utilized to develop compounds with novel modes of action, potentially leading to more effective and environmentally friendly products. Further research is needed to explore its potential in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 899809-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,9,8,0 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 899809-60:
(8*8)+(7*9)+(6*9)+(5*8)+(4*0)+(3*9)+(2*6)+(1*0)=260
260 % 10 = 0
So 899809-60-0 is a valid CAS Registry Number.

899809-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (1R)-4-(diphenylamino)-1-methyl-4-oxo-2-butyn-1-yl ester, (2E)-

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (1R)-4-(diphenylamino)-1-methyl-4-oxo-2-butynyl ester, (2E)-

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:899809-60-0 SDS

899809-60-0Downstream Products

899809-60-0Relevant academic research and scientific papers

EXO- AND DIASTEREO- SELECTIVE SYNTHESES OF HIMBACINE ANALOGS

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Page/Page column 38-39, (2008/06/13)

The application discloses a novel process for the preparation of himbacine analogs useful as thrombin receptor antagonists. The process is based in part on the use of a base-promoted dynamic epimerization of a chiral nitro center. The chemistry taught her

PREPARATION OF CHIRAL PROPARGYLIC ALCOHOL AND ESTER INTERMEDIATES OF HIMBACINE ANALOGS

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Page/Page column 42-43, (2008/06/13)

This application discloses a novel process for the conversion of a series of racemic propargylic alcohols to corresponding (R)-enantiomers. The application also discloses the enantio-selective esterification of a propargylic alcohol from its racemate to p

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