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133342-43-5

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133342-43-5 Usage

General Description

"Phenol, 2-(1,1-dimethylethyl)-6-fluoro-" is a chemical compound that consists of a phenol ring with a 2-tert-butyl and a 6-fluoro substituent. It is commonly used in the pharmaceutical and chemical industries as an intermediate in the synthesis of various organic compounds. This chemical may have potential applications as an ingredient in the manufacturing of pharmaceutical drugs and agrochemicals due to its unique structural properties. It is important to handle this compound with care, as it may have toxic or harmful effects if not properly managed and used in a controlled environment.

Check Digit Verification of cas no

The CAS Registry Mumber 133342-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,4 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133342-43:
(8*1)+(7*3)+(6*3)+(5*3)+(4*4)+(3*2)+(2*4)+(1*3)=95
95 % 10 = 5
So 133342-43-5 is a valid CAS Registry Number.

133342-43-5SDS

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 2-tert-butyl-6-fluorophenol

1.2 Other means of identification

Product number -
Other names Phenol,2-(1,1-dimethylethyl)-6-fluoro

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:133342-43-5 SDS

133342-43-5Upstream product

133342-43-5Downstream Products

133342-43-5Relevant articles and documents

Phenol compound ortho-position direct fluorination method

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Paragraph 0046-0048, (2020/04/17)

The invention relates to a phenol compound ortho-position direct fluorination method which comprises the following steps: reacting a phenol compound shown in a formula (1A) with a fluorination reagentin a solvent under the action of a photocatalyst and a light source at room temperature, and separating and purifying a reaction mixture after the reaction to obtain a fluorinated phenol compound shown in a formula (2A). The advantages are as follows: the method for directly fluorinating phenol by organic photocatalysis is simple in operation process; raw materials are commercialized and easy toobtain; the photocatalyst is low in price, easy to obtain and environmentally friendly; the reaction condition is mild; the site selectivity is high; the reaction is efficient; and a fluorinated phenol derivative can be prepared only through one step.

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