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774213-85-3

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774213-85-3 Usage

Molecular structure

A complex chemical structure derived from indole-3-acetic acid, with additional cyclohexyl and methoxycarbonyl groups.

Natural plant hormone

A synthetic compound based on a natural plant hormone involved in the regulation of plant growth and development.

Steric hindrance

The addition of a cyclohexyl group increases steric hindrance, affecting the compound's interactions with other molecules.

Lipophilicity

The addition of a methoxycarbonyl group increases the compound's lipophilicity, making it more soluble in lipids and potentially more effective as a plant growth regulator or herbicide.

Potential plant growth regulator

Due to its ability to regulate plant growth and development, it may be used as a plant growth regulator or herbicide.

Potential pharmaceutical applications

The presence of a phenyl group suggests potential interactions with biological receptors, making it a subject of interest in medicinal chemistry.

Versatile compound

The unique structure of 1H-Indole-1-acetic acid, 3-cyclohexyl-6-(methoxycarbonyl)-2-phenylmakes it a versatile compound with potential applications in both plant science and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 774213-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,2,1 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 774213-85:
(8*7)+(7*7)+(6*4)+(5*2)+(4*1)+(3*3)+(2*8)+(1*5)=173
173 % 10 = 3
So 774213-85-3 is a valid CAS Registry Number.

774213-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-cyclohexyl-6-methoxycarbonyl-2-phenylindol-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names -

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:774213-85-3 SDS

774213-85-3Relevant articles and documents

Antiviral indoles

-

Page/Page column 7, (2008/12/06)

Compounds of the formula (I): wherein A, B, D, M, Ar, W, X, Y, Z and R1 are as defined herein, are useful in the prevention and treatment of hepatitis C infections. The compounds, their preparation, pharmaceutical compositions containing them and their use in medicine are disclosed.

Development and preliminary optimization of indole-N-acetamide inhibitors of hepatitis C virus NS5B polymerase

Harper, Steven,Pacini, Barbara,Avolio, Salvatore,Di Filippo, Marcello,Migliaccio, Giovanni,Laufer, Ralph,De Francesco, Raffaele,Rowley, Michael,Narjes, Frank

, p. 1314 - 1317 (2007/10/03)

Allosteric inhibition of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase enzyme has recently emerged as a viable strategy toward blocking replication of viral RNA in cell-based systems. We report here a novel class of allosteric inhibitor of NS5B that shows potent affinity for the NS5B enzyme and effective inhibition of subgenomic HCV RNA replication in HUH-7 cells. Inhibitors from this class have promising characteristics for further development as anti-HCV agents.

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