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1-(1-Ethoxy-propyl)-pyrrolidin-2-one is a chemical compound with the molecular formula C8H15NO2. It is a derivative of pyrrolidin-2-one, featuring an ethoxy-propyl group attached to the nitrogen atom. 1-(1-ethoxy-propyl)-pyrrolidin-2-one is an organic molecule that can be used in various chemical reactions and synthesis processes. It is a colorless liquid with a specific molecular weight of 157.21 g/mol. The compound is soluble in organic solvents and has potential applications in the pharmaceutical and chemical industries. Due to its unique structure, it may exhibit specific properties and reactivity, making it a subject of interest for researchers and chemists.

6908-61-8

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6908-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6908-61-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6908-61:
(6*6)+(5*9)+(4*0)+(3*8)+(2*6)+(1*1)=118
118 % 10 = 8
So 6908-61-8 is a valid CAS Registry Number.

6908-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-ethoxy-propyl)-pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names N-(1-Ethoxy-propyl)-pyrrolidon-(2)

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 -
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More Details:6908-61-8 SDS

6908-61-8Downstream Products

6908-61-8Relevant academic research and scientific papers

One-step RhCl3-catalyzed deprotection of acyclic N-allyl amides

Zacuto, Michael J.,Xu, Feng

, p. 6298 - 6300 (2008/02/10)

(Chemical Equation Presented) A convenient one-step RhCl 3-catalyzed deprotection of acyclic N-allyl amides is described. Preliminary mechanistic studies reveal that the key to the success of the one-step deprotection process is the dual function of RhCl3 in alcohol solvents. Reaction of RhCl3 with n-PrOH not only provides an active rhodium hydride species to catalyze isomerization of N-allyl amides to corresponding enamides but also generates a crucial catalytic amount of HCl to convert the enamides to deallylated amides through N,O-acetal exchange.

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