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1-[2,6-bis(1-methylethyl)phenyl]-3-[(2R)-2-(1-methyl-1H-indol-3-yl)hexyl]urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145131-62-0

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145131-62-0 Usage

Classification

Urea derivative

Structure

Contains a phenyl group substituted with two isopropyl groups and a hexyl group attached to a urea moiety through a chiral carbon (2R)

Potential applications

Medicinal chemistry due to its potential biological activities

Biological activities

Interaction with cellular targets or potential as a therapeutic agent

Pharmacological properties

Not explicitly stated, further research needed

Toxicological properties

Not explicitly stated, further research needed

Research status

Further research is needed to fully understand its potential applications and effects
Please note that this list is based on the information provided and may not be exhaustive. Further research and analysis may reveal additional properties and specific content related to 1-[2,6-bis(1-methylethyl)phenyl]-3-[(2R)-2-(1-methyl-1H-indol-3-yl)hexyl]urea.

Check Digit Verification of cas no

The CAS Registry Mumber 145131-62-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,3 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145131-62:
(8*1)+(7*4)+(6*5)+(5*1)+(4*3)+(3*1)+(2*6)+(1*2)=100
100 % 10 = 0
So 145131-62-0 is a valid CAS Registry Number.

145131-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2,6-di(propan-2-yl)phenyl]-3-[(2R)-2-(1-methylindol-3-yl)hexyl]urea

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:145131-62-0 SDS

145131-62-0Downstream Products

145131-62-0Relevant academic research and scientific papers

New indole derivatives as ACAT inhibitors: Synthesis and structure-activity relationships

Bellemin,Decerprit,Festal

, p. 123 - 132 (2007/10/03)

A series of ureas containing the indole group were synthesized and assessed for their ability to inhibit arterial and intestinal ACAT and to lower plasma total cholesterol in a cholesterol-fed rat model. The structural modulations carried out in this series led to compounds which proved to be very active in both the inhibition of aortic ACAT in vitro and the inhibition of rat cholesterol intestinal absorption in vivo. Several compounds from this series exhibit a remarkable hypocholesterolaemic effect with ED25 less than 0.1 mg/kg po.

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