Basic information

Product Name: Cyclopentaneacetamide, N,N-diethyl-
Synonyms:
CAS NO:88931-83-3
Molecular Formula: C11H21NO
Molecular Weight: 183.294
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cyclopentaneacetamide, N,N-diethyl-(CAS DataBase Reference)
NIST Chemistry Reference: Cyclopentaneacetamide, N,N-diethyl-(88931-83-3)
EPA Substance Registry System: Cyclopentaneacetamide, N,N-diethyl-(88931-83-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 88931-83-3(Hazardous Substances Data)

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88931-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88931-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88931-83:
(7*8)+(6*8)+(5*9)+(4*3)+(3*1)+(2*8)+(1*3)=183
183 % 10 = 3
So 88931-83-3 is a valid CAS Registry Number.

88931-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-cyclopentyl-N,N-diethylacetamide

1.2 Other means of identification

Product number	-
Other names	Cyclopentaneacetamide,N,N-diethyl

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:88931-83-3 SDS

88931-83-3Upstream product

88931-82-2 (E)-7-Iodo-hept-2-enoic acid diethylamide

88931-83-3Downstream Products

88931-83-3Relevant academic research and scientific papers

Metal-Halogen Exchange-Initiated Intramolecular Conjugate Addition Reactions of Unsaturated Esters

Cooke, Manning P.

, p. 1144 - 1146 (1984)

Intramolecular conjugate addition reactions of internal unstabilized nucleophilic centers formed through rapid lithium-halogen exchange reactions have been used to generate carbocycles from ω-iodo-α,β-unsaturated esters.

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