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1-Propene, 1-(2-methoxyethoxy)-, (Z)-, also known as Z-1-Propene, 1-(2-methoxyethoxy)-, is an organic chemical compound with the molecular formula C6H12O2. It is a colorless liquid with a density of 0.89 g/cm3 and a boiling point of 120-121°C. 1-Propene, 1-(2-methoxyethoxy)-, (Z)- is characterized by its Z-configuration, indicating the presence of a double bond with the highest priority substituents on the same side of the molecule. It is used as a solvent and a chemical intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its reactivity and potential health hazards, it is important to handle 1-Propene, 1-(2-methoxyethoxy)-, (Z)- with proper safety measures and in accordance with relevant regulations.

62322-42-3

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62322-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62322-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,2 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62322-42:
(7*6)+(6*2)+(5*3)+(4*2)+(3*2)+(2*4)+(1*2)=93
93 % 10 = 3
So 62322-42-3 is a valid CAS Registry Number.

62322-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methoxyethoxy)prop-1-ene

1.2 Other means of identification

Product number -
Other names 1-Propene,1-(2-methoxyethoxy)-,(E)

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:62322-42-3 SDS

62322-42-3Downstream Products

62322-42-3Relevant academic research and scientific papers

Ruthenium-catalyzed selective hydrosilylation reaction of allyl-functionalized PEG derivatives

Inomata, Koya,Naganawa, Yuki,Guo, Haiqing,Sato, Kazuhiko,Nakajima, Yumiko

, (2019)

Reactions of allyl-functionalized poly(ethylene glycol) (PEG) derivatives with alkoxysilanes proceeded efficiently to furnish the corresponding hydrosilylated products in good to excellent yields using a ruthenium catalyst, [RuCl2(nbd)]n. A preliminary mechanistic study supported the pivotal role of the PEG moiety, which coordinated to the ruthenium atom during the reaction to achieve high reaction selectivity. This method may be applicable to the synthesis of various PEGs with a silyl terminus, which is useful as biocompatible and low toxic silane coupling agents.

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