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"2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl 2-iodobenzoate" is a complex organic chemical compound with the molecular formula C16H11IO5. It is characterized by a 2-iodobenzoate group attached to a 2-oxoethyl moiety, which in turn is connected to a 2,3-dihydro-1,4-benzodioxin-6-yl ring. 2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl 2-iodobenzoate is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is typically used as an intermediate in chemical reactions, allowing for the formation of a variety of derivatives with different functional groups. The compound's properties, such as its solubility and stability, can be influenced by the presence of the iodine atom and the benzodioxin ring, making it a versatile building block in organic synthesis.

6052-90-0

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6052-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6052-90-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6052-90:
(6*6)+(5*0)+(4*5)+(3*2)+(2*9)+(1*0)=80
80 % 10 = 0
So 6052-90-0 is a valid CAS Registry Number.

6052-90-0SDS

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-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl] 2-iodobenzoate

1.2 Other means of identification

Product number -
Other names 2,2-Bis-(4-hydroxy-phenyl)-octan

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:6052-90-0 SDS

6052-90-0Downstream Products

6052-90-0Relevant academic research and scientific papers

MANUFACTURING METHOD FOR POLYCARBONATE

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, (2008/06/13)

A method for manufacturing polycarbonate by melt-polycondensing bisphenol and carbonic acid diester uses as catalyst an alkali metal compound and/or alkaline earth metal compound (a). The catalyst is added to the bisphenol prior to the melt polycondensation, in an effective amount, i.e., the amount of alkali metal compound and/or alkaline earth metal compound (a) that acts effectively as a catalyst, is contained in said bisphenol, and is controlled to have the same catalytic activity as 1×10?8 to 1×10?6 mole of bisphenol disodium salt per mole of pure bisphenol A. The method conducts the reaction efficiently from the initial stage in a stable manner to obtain polycarbonate with good color, good heat stability and color stability during molding and the like.

Method for manufacturing bisphenol

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, (2008/06/13)

A method for manufacturing bisphenol by reacting phenols and ketones, characterized (1) in that an alkali metal compound and/or alkaline earth metal compound is added to bisphenol obtained by reacting a phenol and a ketone, and (2) in that the basicity of the bisphenol is adjusted so as to be equivalent to an amount of 1 × 10-8to 1 × 10-6moles of bisphenol as disodium salt with respect to 1 mole of bisphenol provides a bisphenol in which there is no residue of the organic catalysts ordinarily used in manufacturing bisphenol, so that byproducts are not produced during purification, allowing bisphenol with outstanding color tone, thermal resistance, etc., to be obtained.

Process for the purification of bisphenols and preparation of polycarbonates therefrom

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, (2008/06/13)

A phenol and a ketone are reacted to form bisphenol, and the liquid bisphenol obtained or a mixed solution of said solution and a phenol is filtered through a calcined metal filter to obtain bisphenol which makes it possible to efficiently obtain bisphenol which either does not contain fine particulate impurities or contains such impurities only in minute amounts, and a method for manufacturing polycarbonate using bisphenol obtained bythis method. The filtration grade of the calcined metal filter should be 1.0 μm or less. After filtering, the calcined metal filter can be backwashed or chemically washed and then reused. The bisphenol should preferably be bisphenol A.

Processes for producing aromatic polycarbonate oligomer and aromatic polycarbonate

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, (2008/06/13)

A process for producing continuously an aromatic polycarbonate oligomer by reacting an aromatic dihydroxy compound and an alkali metal base or an alkaline earth metal base with a carbonyl halide compound comprises: (1) feeding continuously to a tank reactor an aromatic dihydroxy compound, water, a molecular weight controlling agent, a polymerization catalyst, a carbonyl halide compound, and an organic solvent, and an alkali metal base or an alkaline earth metal base in an amount of 1.15-1.6 equivalents based on the aromatic dihydroxy compound, (2) carrying out the reaction with a residence time as defined by the following formula, where X is an amount of the polymerization catalyst in terms of mole % based on the amount of mole of the aromatic dihydroxy compound fed per unit time, and Y is a residence time (min.), and (3) continuously withdrawing the reaction mixture from the tank reactor to obtain an aromatic polycarbonate oligomer having a number average molecular weight of 1,000-10,000. An aromatic polycarbonate is produced by polycondensation of the aromatic polycarbonate oligomer.

REACTION OF PHENOL WITH 1-OCTYNE IN THE PRESENCE OF ALUMINUM PHENOLATE

Kozlikovskii, Ya. B.,Koshchii, V. A.,Butov, S. A.

, p. 1713 - 1716 (2007/10/02)

The reaction of phenol with 1-octyne in the presence of aluminum phenolate leads to a mixture of the corresponding 2,2-di(hydroxyphenyl)octanes and substituted chromans and chromenes.At temperatures above 160 deg C 2- and 4-(2-octyl)phenols are also forme

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