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78-41-1

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  • Benzeneethanol,4-chloro-a-[4-[2-(diethylamino)ethoxy]phenyl]-a-(4-methylphenyl)-Benzeneethanol,4-chloro-a-[4-[2-(diethylamino)ethoxy]phenyl]-a-(4-methylphenyl)-

    Cas No: 78-41-1

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  • 100 Gram

  • 1000 Kilogram/Month

  • Henan Tianfu Chemical Co., Ltd.
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78-41-1 Usage

Originator

Mer-29,Merrell National,US,1960

Uses

Different sources of media describe the Uses of 78-41-1 differently. You can refer to the following data:
1. Desmosterol Delta 24 (D24) reductase inhibitor
2. Triparanol has been used to inhibit cholesterol biosynthesis in lipid rafts1. Triparanol has also been used as a 3β-hydroxysterol-Δ24-reductase inhibitor to study its effect on delayed-rectifier potassium current (Iks) channels2.

Manufacturing Process

4-(β-diethylaminoethoxy)-4-methylbenzophenone was prepared as follows: a mixture of 200 g of 4-hydroxy-4-methylbenzophenone, 55 g of powdered sodium methoxide and 400 ml of ethanol was stirred for 30 minutes. A solution of 150 g of β-diethylaminoethyl chloride in 300 ml of toluene was added and the mixture was refluxed four hours. The solvent was removed, the residue was taken up in ether, extracted with 5% NaOH solution, twice with water, the ether was removed and the residue was distilled. The product was obtained as an oil boiling at 232°C at 0.6 mm. 1 liter of a 0.45 N ethereal solution of p-chlorobenzyl magnesium chloride was added in 30 minutes to a stirred solution of 104 g (0.35 mol) of 4-(β- diethylaminoethoxy)-4-methylbenzophenone in 400 ml of dry ether. After stirring an additional hour, the mixture was decomposed by pouring onto 1 liter of cold 10% ammonium chloride solution, the ether solution was washed with water, and the ether was replaced with hot isopropanol containing a trace of ammonia. 1-[p-(β-diethylaminoethoxy)phenyl]-1-phenyl-2-p-tolyl-2-p_x0002_chloroethanol separated as white crystals, melting at 104% to 106°C.

Therapeutic Function

Antihyperlipidemic

Biochem/physiol Actions

Triparanol is known to repress Hedgehog signaling in cancer cells and can also inhibit tumor growth3.

Check Digit Verification of cas no

The CAS Registry Mumber 78-41-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78-41:
(4*7)+(3*8)+(2*4)+(1*1)=61
61 % 10 = 1
So 78-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H32ClNO2/c1-4-29(5-2)18-19-31-26-16-12-24(13-17-26)27(30,23-10-6-21(3)7-11-23)20-22-8-14-25(28)15-9-22/h6-17,30H,4-5,18-20H2,1-3H3

78-41-1 Well-known Company Product Price

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  • Sigma

  • (T5200)  Triparanol  ≥97% (HPLC), powder

  • 78-41-1

  • T5200-5MG

  • 1,698.84CNY

  • Detail
  • Sigma

  • (T5200)  Triparanol  ≥97% (HPLC), powder

  • 78-41-1

  • T5200-25MG

  • 6,499.35CNY

  • Detail

78-41-1SDS

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-(4-chlorophenyl)-1-[4-[2-(diethylamino)ethoxy]phenyl]-1-(4-methylphenyl)ethanol

1.2 Other means of identification

Product number -
Other names Metasqualene

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:78-41-1 SDS

78-41-1Downstream Products

78-41-1Relevant articles and documents

From Anilines to Aryl Ethers: A Facile, Efficient, and Versatile Synthetic Method Employing Mild Conditions

Wang, Dong-Yu,Yang, Ze-Kun,Wang, Chao,Zhang, Ao,Uchiyama, Masanobu

supporting information, p. 3641 - 3645 (2018/03/13)

We have developed a simple and direct method for the synthesis of aryl ethers by reacting alcohols/phenols (ROH) with aryl ammonium salts (ArNMe3+), which are readily prepared from anilines (ArNR′2, R′=H or Me). This reaction proceeds smoothly and rapidly (within a few hours) at room temperature in the presence of a commercially available base, such as KOtBu or KHMDS, and has a broad substrate scope with respect to both ROH and ArNR′2. It is scalable and compatible with a wide range of functional groups.

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