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1-phenyl-2-propoxy-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4249-43-8

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4249-43-8 Usage

Physical properties

Clear, slightly yellowish liquid with a mild odor

Usage

Sedative and anesthetic agent in medical settings

Administration

Typically administered intravenously

Mechanism of action

Depresses the central nervous system, resulting in sedation and loss of consciousness

Common uses

Minor procedures and sedation of critically ill patients in intensive care units

Risks

Respiratory depression and lowered blood pressure, should only be administered under the supervision of trained medical professionals

Legal status

Controlled substance due to potential for abuse and diversion.

Check Digit Verification of cas no

The CAS Registry Mumber 4249-43-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4249-43:
(6*4)+(5*2)+(4*4)+(3*9)+(2*4)+(1*3)=88
88 % 10 = 8
So 4249-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O2/c1-2-8-13-9-11(12)10-6-4-3-5-7-10/h3-7,11-12H,2,8-9H2,1H3

4249-43-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-2-propoxyethanol

1.2 Other means of identification

Product number -
Other names 1-PHENYL-2-PROPOXY-ETHANOL

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:4249-43-8 SDS

4249-43-8Upstream product

4249-43-8Downstream Products

4249-43-8Relevant academic research and scientific papers

Aerobic Photooxidative Synthesis of β-Alkoxy Monohydroperoxides Using an Organo Photoredox Catalyst Controlled by a Base

Asano, Yuya,Nagasawa, Yoshitomo,Yamaguchi, Eiji,Itoh, Akichika

, p. 409 - 412 (2018/02/21)

Transition-metal-free synthesis of β-alkoxy monohydroperoxides via aerobic photooxidation using an acridinium photocatalyst was developed. This method enables the synthesis of some novel hydroperoxides. The peroxide source is molecular oxygen, which is cost-effective and atomically efficient. Magnesium oxide plays an important role as a base in the catalytic system.

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