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14066-72-9

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14066-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14066-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,6 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14066-72:
(7*1)+(6*4)+(5*0)+(4*6)+(3*6)+(2*7)+(1*2)=89
89 % 10 = 9
So 14066-72-9 is a valid CAS Registry Number.

14066-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylpentan-2-ylideneamino)urea

1.2 Other means of identification

Product number -
Other names 1-(4-METHYL-2-PENTYLIDENE)SEMICARBAZIDE

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:14066-72-9 SDS

14066-72-9Relevant articles and documents

1,2,3-Selenadiazole-driven single family MSNCs of CdSe

Jadhav, Aditi A.,Khanna, Pawan K.

, p. 14713 - 14722 (2017/11/28)

Herein, 1,2,3-selenadiazoles were instantly prepared by hand grinding the reactants via a solventless process and tested for their ability to act as a source of selenium for the synthesis of CdSe magic-sized nanoclusters (MSNCs) with size below 2 nm. The

Reactions of diazoalkanes with isocyanates. Synthesis of imidazolidine-2,4-diones, oxindoles, and oxazolidinones

Fulton, Janet B.,Warkentin, John

, p. 1177 - 1184 (2007/10/02)

Thermolysis of a 5,5-dialkyl-Δ3-1,3,4-oxadiazolin-2-one in nitrobenzene containing an aryl isocyanate at 150 deg C affords a 1,3-diaryl-5,5-dialkyl imidazolidine-2,4-dione, an N-arylcarbamoyl-3,3-dialkyloxindole, and a 3-aryl-2-arylimino-5,5-dialkyl-1,3-oxazolidin-4-one.Those products arise from attack of a diazoalkane, generated in situ from the oxadiazolinone by thermal cycloreversion, on the isocyanate function.Two imidazolidine diones, three oxazolidinones, and 14 oxindoles were prepared.

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