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Phenol, 4-[1-(4-methoxyphenyl)-1-methylethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16530-58-8 Structure
  • Basic information

    1. Product Name: Phenol, 4-[1-(4-methoxyphenyl)-1-methylethyl]-
    2. Synonyms:
    3. CAS NO:16530-58-8
    4. Molecular Formula: C16H18O2
    5. Molecular Weight: 242.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16530-58-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Phenol, 4-[1-(4-methoxyphenyl)-1-methylethyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 4-[1-(4-methoxyphenyl)-1-methylethyl]-(16530-58-8)
    11. EPA Substance Registry System: Phenol, 4-[1-(4-methoxyphenyl)-1-methylethyl]-(16530-58-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 16530-58-8(Hazardous Substances Data)

16530-58-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16530-58-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,3 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16530-58:
(7*1)+(6*6)+(5*5)+(4*3)+(3*0)+(2*5)+(1*8)=98
98 % 10 = 8
So 16530-58-8 is a valid CAS Registry Number.

16530-58-8SDS

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 4-[2-(4-methoxyphenyl)propan-2-yl]phenol

1.2 Other means of identification

Product number -
Other names 4-[1-(4-methoxy-phenyl)-1-methyl-ethyl]-phenol

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:16530-58-8 SDS

16530-58-8Relevant articles and documents

Lithium doped TiO2 as catalysts for the transesterification of bisphenol-A with dimethyl carbonate

Liang, Yanan,Su, Kunmei,Cao, Lei,Li, Zhenhuan

, p. 16 - 23 (2019/01/04)

Lithium doped TiO2 were prepared by simple impregnation, which was used as heterogeneous catalysts for the transesterification of DMC with BPA. The characterized results of FTIR, XRD, XPS, SEM, TEM and temperature programmed desorption of CO2 (CO2-TPD) showed that the structure and performance of the catalysts were obviously influenced by the doping amount of Li+ and calcining temperature. The optimum catalytic activity was obtained when the molar ratio of Ti/Li reached 6 and the calcination temperature came up to 400 ℃ which was due to Li+ reaction with TiO2 to form surface Ti-O-Li at 400 ℃ (Ti/Li-6-400). When the transesterification of DMC with BPA was carried out at 160–180 ℃ over Ti/Li-6-400, BPA conversion reached 46.67%, and the yields of one-methylcarbonate-ended-BPA (MmC(1)) and two-methylcarbonate-ended-BPA (DmC(1)) achieved 36.36% and 5.97%, respectively, and only 9.3% methylation selectivity was detected. In addition, the possible transesterification mechanism was provided.

Study on the transesterification and mechanism of bisphenol A and dimethyl carbonate catalyzed by organotin oxide

Liang, Yanan,Su, Kunmei,Cao, Lei,Gao, Yuan,Li, Zhenhuan

, p. 2171 - 2182 (2019/06/21)

(CF3C6H4)2SnO, (CH3C6H4)2SnO and Ph2SnO were successfully synthesized for the transesterification of DMC with BPA. The products of mono-methylcarbonate-ended-BPA (MmC(1)) and two-methylcarbonate-ended-BPA (DmC(1)) were selectively synthesizedthem. The catalysts were characterized by FT-IR, TG and XPS. When Ph2SnO was used as the catalyst at 170?°C, the BPA conversion reached to 28.60% and the transesterification selectivity reached to 98.35%. As for (CF3C6H4)2SnO, BPA conversion and transesterification selectivity declined to 12.48% and 64.74%, respectively. The BPA conversion increased to 42.83%, but the transesterification selectivity declined to 44.55%(CF3C6H4)2SnO. Notability, the higher transesterification selectivity of Ph2SnO was due to its lowest electron binding energy of Sn4+. More importantly, the DMC adsorption, activation and decomposition process(CF3C6H4)2SnO, (CH3C6H4)2SnO and Ph2SnO were characterized by TG–MS and in situ DRIFT techniques, which provided more information about the mechanism of transesterification and methylation.

METHODS OF MANUFACTURE OF SALTS OF HYDROXY-SUBSTITUTED AROMATIC COMPOUNDS AND POLYETHERIMIDES

-

Paragraph 0042; 0043, (2015/11/09)

A method for the manufacture of a metal salt of a hydroxy-substituted aromatic compound comprises: contacting a hydroxy-substituted aromatic compound with a base comprising a metal cation in molten diphenyl sulfone or sulfolane to provide a mixture compri

Study on the reaction between bisphenol A and dimethyl carbonate over organotin oxide

He, Xiaolong,Li, Zhenhuan,Su, Kunmei,Cheng, Bowen,Ming, Jun

, p. 20 - 23 (2013/05/09)

Organotin oxide was used to catalyze the reaction between BPA (bisphenol A) and DMC (dimethyl carbonate), and Ph2SnO (diphenyltin oxide) displays the excellent catalytic performance in transesterification and O-methylation. However, Bu2SnO (dibutyltin oxide), (PhCH 2)2SnO (dibenzyltin oxide) and (C6H 11)2SnO (dicyclohexyltin oxide) exhibited weaker catalytic activity but higher selectivity for C-methylation product formation. The π-π function between Ph2SnO and BPA provided more chances for their interaction, and π-d interaction between phenyl ring and Sn resulted in catalyst having higher activity in transesterification and O-methylation. O-methylation product formation over Ph2SnO comes from transesterification product decomposition not from direct methylation of BPA with DMC.

Hydrosilanes are not always reducing agents for carbonyl compounds, II: Ruthenium-catalyzed deprotection of tert-butyl groups in carbamates, carbonates, esters, and ethers

Hanada, Shiori,Yuasa, Akihiro,Kuroiwa, Hirotaka,Motoyama, Yukihiro,Nagashima, Hideo

supporting information; experimental part, p. 1021 - 1025 (2010/04/27)

Hydrosilanes act as a reagent to cleave the C-O bond of OtBu groups in carbamates, carbonates, esters, and ethers by catalysis of a triruthenium cluster. The reaction offers a novel deprotection method, for OiBu groups under neutral conditions, showing unique selectivities that have never been accomplished with conventional Bronsted or Lewis acidic promoters. Possible mechanisms for C-O cleavage are discussed on the basis of NMR spectroscopic analysis.

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