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Benzenemethanol, 2-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-α-propyl-, is a complex organic compound with the chemical formula C13H18NO2. It is a derivative of benzenemethanol, featuring a 4,5-dihydro-4,4-dimethyl-2-oxazolyl group attached to the α-carbon of the propyl chain. This molecule is characterized by its unique structure, which includes a benzene ring, a hydroxyl group, and a 2-oxazolyl moiety. It is synthesized through a series of chemical reactions and is used in various applications, such as in the pharmaceutical industry for the development of drugs and in the synthesis of other complex organic molecules. Due to its specific functional groups and structural features, it exhibits unique chemical properties and reactivity, making it an important compound in organic chemistry research and development.

88440-92-0

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88440-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88440-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,4 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88440-92:
(7*8)+(6*8)+(5*4)+(4*4)+(3*0)+(2*9)+(1*2)=160
160 % 10 = 0
So 88440-92-0 is a valid CAS Registry Number.

88440-92-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-<2-(1-Hydroxybutyl)phenyl>-4,4-dimethyloxazoline

1.2 Other means of identification

Product number -
Other names 1-[2-(4,4-Dimethyl-4,5-dihydro-oxazol-2-yl)-phenyl]-butan-1-ol

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:88440-92-0 SDS

88440-92-0Downstream Products

88440-92-0Relevant academic research and scientific papers

Group exchange between ketones and carboxylic acids through directing group assisted Rh-catalyzed reorganization of carbon skeletons

Lei, Zhi-Quan,Pan, Fei,Li, Hu,Li, Yang,Zhang, Xi-Sha,Chen, Kang,Wang, Xin,Li, Yu-Xue,Sun, Jian,Shi, Zhang-Jie

supporting information, p. 5012 - 5020 (2015/05/05)

The Rh(I)-catalyzed direct reorganization of organic frameworks and group exchanges between carboxylic acids and aryl ketones was developed with the assistance of directing group. Biaryls, alkenylarenes, and alkylarenes were produced in high efficiency from aryl ketones and the corresponding carboxylic acids by releasing the other molecule of carboxylic acids and carbon monoxide. A wide range of functional groups were well compatible. The exchanges between two partners were proposed to take place on the Rh-(III) center of key intermediates, supported by experimental mechanistic studies and computational calculations. The transformation unveiled the new catalytic pathway of the group transfer of two organic molecules.

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