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4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10073-86-6

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10073-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10073-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,7 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10073-86:
(7*1)+(6*0)+(5*0)+(4*7)+(3*3)+(2*8)+(1*6)=66
66 % 10 = 6
So 10073-86-6 is a valid CAS Registry Number.

10073-86-6SDS

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 2-phenyl-5,5-dimethyl-1,3-oxazine-4,6-dione

1.2 Other means of identification

Product number -
Other names 5,5-Dimethyl-2-phenyl-4H-1,3-oxazine-4,6(5H)-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:10073-86-6 SDS

10073-86-6Relevant academic research and scientific papers

Reaction of Dimethyl- and Diethylmalonyl Dichlorides with Aromatic Amides

Yakovlev,Zakhs,Prep'yalov,Rebrov

, p. 650 - 652 (2007/10/03)

Dimethylmalonyl dichloride reacts with substituted benzamides with formation of mixtures of 2-aryl-5,5-dimethyl-1,3-oxazine-4,6-diones and N,N'-bis(aroyl)dimethylmalonediamides whose ratio depends on the reactant concentration. Under similar conditions, diethylmalonyl dichloride with the same amides gives only N,N'-bis(aroyl)diethylmalonediamides.

AZOLES AND AZINES. 62. STRUCTURE OF 2-ARYL-1,3-OXAZINE-4,6-DIONES

Zakhs, V. E.,Yakovlev, I. P.,Smorygo, N. A.,Gindin, V. A.,Ivin, B. A.

, p. 325 - 332 (2007/10/02)

1H, 13C NMR, IR, and UV spectra have been studied for solutions of a number of potentially tautomeric 2-aryl-1,3-oxazine-4,6-diones and their 5-methyl substituted analogs with variation of substitutent at the para position of the benzene ring, as well as compounds with a fixed structure that simulates possible tautomeric forms.The data have been compared with the results of quantum chemical calculations carried out in SSO MO LCAO approximation by the CNO, CNDO/2, and MPNDO/3 methods.In DMSO and THF solution the test compounds exist predominantly as 2-aryl-4-hydroxy-6H-1,3-oxazin-6-ones.The para substituent in the benzene ring does not effect the composition of the tautomer mixture significantly.

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