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81266-47-9

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81266-47-9 Usage

General Description

3-(Nitromethyl)cyclopentanone is an organic compound that falls under the category of a ketone. It consists of a cyclopentanone ring -- a five-member cycloalkane that includes one oxygen atom, and hence, a ketone -- that is substituted with a nitromethyl functional group at the 3-position. Its exact molecular structure, weight, and formula are subject to specific measurement and detection techniques. It can be potentially used in various chemical reactions and syntheses in laboratories. Due to its nitro group, it may also require precautionary handling and storage due to potential reactivity. Clear information about its safety, toxicity, or potential hazards should be referred from a Material Safety Data Sheet (MSDS).

Check Digit Verification of cas no

The CAS Registry Mumber 81266-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,6 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81266-47:
(7*8)+(6*1)+(5*2)+(4*6)+(3*6)+(2*4)+(1*7)=129
129 % 10 = 9
So 81266-47-9 is a valid CAS Registry Number.

81266-47-9SDS

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 3-(Nitromethyl)cyclopentanone

1.2 Other means of identification

Product number -
Other names 3-(nitromethyl)cyclopentan-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:81266-47-9 SDS

81266-47-9Relevant articles and documents

Arginine- or lysine-catalyzed Michael addition of nitromethane to α,β-unsaturated ketones in aqueous media

Park, Seongsoon

, p. 3671 - 3674 (2015/02/05)

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Asymmetric conjugate addition of nitroalkanes to enones with a chiral α-aminophosphonate catalyst

Malmgren, Marcus,Granander, Johan,Amedjkouh, Mohamed

, p. 1934 - 1940 (2008/12/22)

Chiral diethyl (2R)-tetrahydropyrro-2-ylphosphonate is an effective catalyst for the Michael addition of nitroalkanes to α,β-unsaturated ketones. This study revealed that the hydrate salt of this α-aminophosphonate was found to be a better catalytic speci

CONJUGATE ADDITION OF ALIPHATIC NITRO COMPOUNDS TO 2-CYCLOPENTENONE

Kadas, I.,Morvai-Kadas, V.,Toeke, L.

, p. 303 - 308 (2007/10/02)

Conjugate addition of aliphatic nitro compounds to 2-cyclopentenone has been studied.The best results were obtained by the application of nitronate anions, prepared in situ with methanolic sodium methoxide solution.The adducts have been characterized by elemental analysis and spectroscopic data.

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