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1989-04-4

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1989-04-4 Usage

General Description

4-[1-(4-chlorophenyl)-1-methylethyl]phenol is a chemical compound that contains a benzene ring with a hydroxyl group and a 4-chlorophenyl group attached to it. The compound also has a 1-methylethyl group attached to the benzene ring. It is commonly used in the manufacturing of pharmaceuticals, including as an intermediate in the synthesis of other compounds. It may also be used as a reagent in chemical reactions and as a building block in the production of various organic compounds. 4-[1-(4-CHLOROPHENYL)-1-METHYLETHYL]PHENOL is known to have potential biological activity and may have applications in the development of new drugs and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1989-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1989-04:
(6*1)+(5*9)+(4*8)+(3*9)+(2*0)+(1*4)=114
114 % 10 = 4
So 1989-04-4 is a valid CAS Registry Number.

1989-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-chlorophenyl)propan-2-yl]phenol

1.2 Other means of identification

Product number -
Other names F0701-0003

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:1989-04-4 SDS

1989-04-4Downstream Products

1989-04-4Relevant articles and documents

Catalytic Hydroarylation of Alkenes with Phenols using B(C6F5)3

Bentley, Jordan N.,Caputo, Christopher B.

supporting information, p. 3654 - 3658 (2018/10/20)

We demonstrate that tris(pentafluorophenyl)borane, B(C6F5)3, is shown to be an effective catalyst for the hydroarylation of olefins to yield substituted phenols. This system features fast reaction times, mild conditions, and good yields for a select scope of olefinic substrates and various phenols, resulting in C-C bond formation. Experimental data support two possible mechanisms, where the Lewis acid can activate either the olefin or the phenol as the first step in the catalytic mechanism.

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