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95338-32-2

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95338-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95338-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,3 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95338-32:
(7*9)+(6*5)+(5*3)+(4*3)+(3*8)+(2*3)+(1*2)=152
152 % 10 = 2
So 95338-32-2 is a valid CAS Registry Number.

95338-32-2SDS

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-nitrocyclododecanone

1.2 Other means of identification

Product number -
Other names 2-nitro cyclododecan-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:95338-32-2 SDS

95338-32-2Relevant articles and documents

A novel one pot synthesis of α-nitroketones from olefins using trimethylsilylnitrate-chromium trioxide reagent system

Reddy, M. Venkat Ram,Kumareswaran,Vankar, Yashwant D.

, p. 7149 - 7152 (1995)

A variety of α-nitroketones have been obtained from the corresponding olefins in good yields upon reaction with trimethylsilylnitrate-chromium trioxide reagent system.

Practical and User-Friendly Procedure for Michael Reactions of α-Nitroketones in Water

Miranda, Sonia,López-Alvarado, Pilar,Giorgi, Giorgio,Rodriguez, Jean,Avenda?o, Carmen,Menéndez, J. Carlos

, p. 2159 - 2162 (2007/10/03)

A variety of α,β-unsaturated carbonyl derivatives gave selective Michael additions with several α-nitrocycloalkanones in water, at room temperature without any added catalyst, or in very dilute, aqueous solutions of potassium carbonate. Both preparative methods constitute new, environmentally benign and more efficient alternatives to previous procedures.

Syntheses of macrocyclic lactones by ring enlargement reaction. Preparation of (±)-phoracantholide I, (±)-dihydrorecifeiolide and (±)-15-hexadecanolide

Kostova,Hesse

, p. 1713 - 1724 (2007/10/02)

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