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Phenol, 2-methyl-6-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53621-45-7

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53621-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53621-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,2 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53621-45:
(7*5)+(6*3)+(5*6)+(4*2)+(3*1)+(2*4)+(1*5)=107
107 % 10 = 7
So 53621-45-7 is a valid CAS Registry Number.

53621-45-7SDS

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-Isopropenyl-6-methyl-phenol

1.2 Other means of identification

Product number -
Other names β-(2-Oxy-3-methyl-phenyl)-propylen

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:53621-45-7 SDS

53621-45-7Relevant academic research and scientific papers

BISPHENOL COMPOSITION AND POLYCARBONATE RESIN

-

, (2022/04/03)

A bisphenol composition includes 95% or more by mass of a bisphenol and 200 mass ppm or more of a compound represented by the following general formula (II): In formula (II), R21 and R22 denote a methyl group or a hydrogen atom; R22 is a methyl group when R21 is a hydrogen atom; R22 is a hydrogen atom when R21 is a methyl group; R23 to R25 independently denote a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; and R23, R24, and R25 may be bonded or cross-linked between two of the groups. A method for producing a polycarbonate resin using the bisphenol composition is also described.

Iridium-Catalyzed C(sp3)?H Addition of Methyl Ethers across Intramolecular Carbon–Carbon Double Bonds Giving 2,3-Dihydrobenzofurans

Ohmura, Toshimichi,Kusaka, Satoshi,Torigoe, Takeru,Suginome, Michinori

supporting information, p. 4448 - 4453 (2019/09/16)

Intramolecular addition of an O-methyl C(sp3)?H bond across a carbon-carbon double bond occurs in the iridium-catalyzed reaction of methyl 2-(propen-2-yl)phenyl ethers. The Ir/(S)-DTBM-SEGPHOS catalyst promotes the reaction efficiently in toluene at 110–135 °C to afford 3,3-dimethyl-2,3-dihydrobenzofurans. Enantioselective C(sp3)?H addition is achieved in the reaction of methyl 2-(1-siloxyethenyl)phenyl ethers, affording enantioenriched 3-hydroxy-2,3-dihydrobenzofuran derivatives with up to 96% ee. (Figure presented.).

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