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5820-02-0

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5820-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5820-02-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5820-02:
(6*5)+(5*8)+(4*2)+(3*0)+(2*0)+(1*2)=80
80 % 10 = 0
So 5820-02-0 is a valid CAS Registry Number.

5820-02-0SDS

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 ethyl 7-methyl-2-[[5-(4-methyl-2-nitrophenyl)furan-2-yl]methylidene]-5-(4-methylsulfanylphenyl)-3-oxo-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-4,4-diphenylbut-3-enal

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:5820-02-0 SDS

5820-02-0Relevant articles and documents

Novel photochemical behaviour of the oximes and hydrazones of β,γ-unsaturated carbonyl compounds

Armesto, Diego,Ramos, Ana,Ortiz, Maria J.,Horspool, William M.,Mancheno, Maria J.,Caballero, Olga,Mayoral, Elena P.

, p. 1535 - 1541 (2007/10/03)

A study of the photochemical reactivity of a series of β,γ-unsaturated oximes and hydrazone derivatives under triplet sensitized conditions has been carried out. The oximes 3c, 4a and 4c cyclize to the corresponding dihydroisoxazoles 5c, 6a and 6c while t

Substitution Effects on the Aza-di-?-methane Rearrangement of Imines

Armesto, Diego,Horspool, William M.,Langa, Fernando,Perez-Ossorio, Rafael

, p. 1039 - 1042 (2007/10/02)

The u.v. irradiation of several 1-aryl derivatives of 3,3-dimethyl-5,5-diphenyl-1-azapenta-1,4-diene has been carried out.All of them undergo the aza-di-?-methane rearrangement and yield a cyclopropylimine.The influence of substituents on the 1-aryl group has given support for the proposal that imines with a low ionization potential are less efficient at undergoing the aza-di-?-methane process than imines with a higher ionization potential.This was demonstrated in a quantitative fashion.The involvement of an electron-transfer process in the reaction is discussed.

A NOVEL AZA-DI-?-METHANE REARRANGEMENT THE PHOTOREACTION OF 4,4-DIMETHYL-1,6,6-TRIPHENYL-2-AZA-HEXA-2,5-DIENE

Armesto, Diego,Martin, Juan Antonio F.,Perez-Ossorio, Rafael

, p. 2149 - 2152 (2007/10/02)

The synthesis and the novel photochemical aza-di-?-methane reaction of 4,4-dimethyl-1,6,6-triphenyl-2-aza-hexa-2,5-diene are described.

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