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129441-80-1

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129441-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129441-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,4,4 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129441-80:
(8*1)+(7*2)+(6*9)+(5*4)+(4*4)+(3*1)+(2*8)+(1*0)=131
131 % 10 = 1
So 129441-80-1 is a valid CAS Registry Number.

129441-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-oxocyclopent-2-en-1-yl)benzamide

1.2 Other means of identification

Product number -
Other names 4-benzoylamino-2-cyclopenten-1-one

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:129441-80-1 SDS

129441-80-1Relevant articles and documents

Intra- and intermolecular hydrogen bonding effects in cycloadditions between nitrile oxides and 4-benzoylamino-2-cyclopenten-1-ol and its derivatives

Quadrelli, Paolo,Fassardi, Vera,Cardarelli, Annamaria,Caramella, Pierluigi

, p. 2058 - 2065 (2007/10/03)

Cycloadditions between nitrile oxides and cis-4-benzoylamino-2-cyclopenten-1-ol offer an example in which a strong intramolecular hydrogen bond completely offsets the syn-directing ability of the cyclopentene substituents. Solvents affected the conformational equilibrium of the cyclopentene dipolarophile but did not sizeably influence the cycloaddition selectivity, showing the absence of directing effects between the addends. Removal of the intramolecular hydrogen bond by OH protection or oxidation activated the syn-directing ability of the amido substituent and provided a convenient route to syn stereoselection. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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