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Benzenemethanol, 3-(2,2-dimethoxy-1-methylethyl)-α-phenyl-, also known as 3-(2,2-dimethoxy-1-methylethyl)-α-phenylbenzenemethanol, is an organic compound with the chemical formula C16H22O3. It is a derivative of benzenemethanol, featuring a 2,2-dimethoxy-1-methylethyl group attached to the 3-position of the benzene ring and an α-phenyl group at the 1-position. Benzenemethanol, 3-(2,2-dimethoxy-1-methylethyl)-a-phenyl- is characterized by its unique molecular structure, which includes a benzene ring, a hydroxyl group, and a substituted ethyl group. It is a colorless liquid with a specific molecular weight of 262.35 g/mol. This chemical is primarily used in the synthesis of pharmaceuticals and other organic compounds due to its versatile structure and reactivity.

89539-11-7

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89539-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89539-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89539-11:
(7*8)+(6*9)+(5*5)+(4*3)+(3*9)+(2*1)+(1*1)=177
177 % 10 = 7
So 89539-11-7 is a valid CAS Registry Number.

89539-11-7SDS

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-(3-(α-hydroxybenzyl)phenyl)propanal dimethyl acetal

1.2 Other means of identification

Product number -
Other names 2-[3-(α-hydroxybenzyl)phenyl]propanal dimethyl acetal

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89539-11-7 SDS

89539-11-7Upstream product

89539-11-7Downstream Products

89539-11-7Relevant academic research and scientific papers

A Simple and Efficient Conversion of Aldehyde Acetals into Esters

Sugai, Saburo,Kodama, Takashi,Akaboshi, Sanya,Ikegami, Shiro

, p. 99 - 105 (2007/10/02)

The reaction of aldehydic acetals with hypochlorous acid in acetic acid-acetone afforded the corresponding esters in excellent yields.From cyclic acetals, only the corresponding hydroxyalkyl esters were obtained.Keywords - acetal; hypochlorite; hypochlorous acid; conversion; ester; hydroxyalkyl ester; regioselectivity

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