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111149-62-3

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111149-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111149-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,4 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111149-62:
(8*1)+(7*1)+(6*1)+(5*1)+(4*4)+(3*9)+(2*6)+(1*2)=83
83 % 10 = 3
So 111149-62-3 is a valid CAS Registry Number.

111149-62-3SDS

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 Chalcone oxime

1.2 Other means of identification

Product number -
Other names 4-chloro-chalcone oxime

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:111149-62-3 SDS

111149-62-3Upstream product

111149-62-3Relevant articles and documents

An improved, efficient and microwave assisted synthetic method for the synthesis of chalcone oximes: An experimental and computational study

Erdogan, Taner,Erdogan, Fatma Oguz

, p. 99 - 110 (2018/03/06)

Chalcone oximes are important molecules in organic chemistry. Extant literature contains several methods for conversion of chalcones to their oxime forms but rapid and efficient new methods need to be developed. In this study; we have investigated a new, microwave assisted synthetic method for conversion of chalcones to their oxime forms. For this purpose, a series of known chalcones were synthesized and converted to their oxime forms employing the method being examined. The results show that the proposed method is efficient, providing time and energy savings. In the second part of our study, DFT calculations with B3LYP method have been performed on the synthesized molecules and computational results have been compared with the experimentally obtained data. All DFT calculations were performed at the B3LYP/6-31G(d), B3LYP/6-311G(d, p) and B3LYP/6-311+G(2d, p) levels of theory. NMR calculations were carried out using GIAO and CSGT methods. Additionally, MEP maps, FMOs, some global reactivity descriptors and Mulliken atomic charges for the synthesized compounds were computationally determined with the same basis sets.

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