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129222-15-7

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129222-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129222-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129222-15:
(8*1)+(7*2)+(6*9)+(5*2)+(4*2)+(3*2)+(2*1)+(1*5)=107
107 % 10 = 7
So 129222-15-7 is a valid CAS Registry Number.

129222-15-7SDS

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 2-acetyl-hexahydro-cyclopenta[c]pyrrol-5-one

1.2 Other means of identification

Product number -
Other names 2-Acetyl-hexahydro-cyclopenta[c]pyrrol-5-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:129222-15-7 SDS

129222-15-7Downstream Products

129222-15-7Relevant articles and documents

DERIVATIVES OF AZABICYCLO OCTANE, THE METHOD OF MAKING THEM AND THE USES THEREOF AS INHIBITORS OF DIPEPTIDYL PEPTIDASE IV

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Page/Page column 19-20, (2009/12/27)

Derivatives of azabicyclo octane presented by formula (I), the method of making them, and the compositions containing the same and the uses thereof as inhibitors of dipeptidyl peptidase IV (DPP-IV), wherein the substitutes in formula (I) have the same meanings as what is mentioned in the descriptions.

The Synthesis of Nitrogen Heterocycles via the Intramolecular Khand Reaction: Formation of Tetra- and Hexa-hydrocyclopentapyrrol-5(1H)-ones and Hexahydro-6H-2-pyrindin-6-ones

Brown, Scott W.,Pauson, Peter L.

, p. 1205 - 1209 (2007/10/02)

Azabicyclooctenones and azabicyclononenones have been obtained by cyclisation of hexacarbonyldicobalt complexes of aza-heptenynes and -octenynes respectively.An unusual feature of the cyclisation of N-acyl-4-azahept-1-en-6-ynes is the extens

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