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5564-44-3

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5564-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5564-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5564-44:
(6*5)+(5*5)+(4*6)+(3*4)+(2*4)+(1*4)=103
103 % 10 = 3
So 5564-44-3 is a valid CAS Registry Number.

5564-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[1-(3-chlorophenyl)-1-oxopropan-2-yl]-5,5-diphenylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-[(2R)-1-(3-chlorophenyl)-1-oxopropan-2-yl]-5,5-diphenylimidazolidine-2,4-dione

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:5564-44-3 SDS

5564-44-3Relevant articles and documents

Mechanism of thermal deazetization of 2,3-diazabicyclo[2.2.1]hept-2-ene and its reaction dynamics in supercritical fluids

Reyes, Mayra B.,Carpenter, Barry K.

, p. 10163 - 10176 (2000)

The mechanism of thermal deazetization of 2,3-diazabicyclo[2.2.1]hept-2-ene (DBH) is examined both theoretically and experimentally in this paper. The theoretical work involves CASPT2 ab initio MO calculations using the 6-31G(d) basis set. These calculati

Expanding the scope of methyl xanthate esters - From Barton-McCombie reaction auxiliary to versatile protective group

Thorsheim, Karin,Manner, Sophie,Ellervik, Ulf

supporting information, p. 6329 - 6333 (2017/09/29)

The methyl xanthate ester is presented as a versatile protective group for alcohols. Hydroxyl groups can easily be transformed into methyl xanthate esters by several methods and are commonly used as an auxiliary in the Barton-McCombie reaction. We show that these methyl xanthate esters can readily and chemoselectively be cleaved under mild conditions by the action of diethylenetriamine using microwave heating. This method is orthogonal to many common hydroxyl protective groups that can be introduced and cleaved in the presence of methyl xanthate ester.

Mild and efficient synthesis of thiocarbonates and thiocarbamates via a three-component coupling utilizing Cs2CO3 and TBAI

Salvatore, Ralph N.,Sahab, Suma,Jung, Kyung Woon

, p. 2055 - 2058 (2007/10/03)

The presence of cesium carbonate and tetrabutylammonium iodide (TBAI) facilitated efficient thiocarbonylation of alcohols, and thiocarbamation of amines, using carbon disulfide with alkyl halides. This protocol was mild, chemoselective, and efficient, compared to the existing methods.

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