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19073-15-5

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19073-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19073-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19073-15:
(7*1)+(6*9)+(5*0)+(4*7)+(3*3)+(2*1)+(1*5)=105
105 % 10 = 5
So 19073-15-5 is a valid CAS Registry Number.

19073-15-5SDS

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 2-methyl-2-(4-nitrophenyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 2-methyl-2-(4-nitro-phenyl)-[1,3]-dioxolane

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:19073-15-5 SDS

19073-15-5Relevant articles and documents

Catalytic application of sulfamic acid-functionalized magnetic Fe3O4nanoparticles (SA-MNPs) for protection of aromatic carbonyl compounds and alcohols: Experimental and theoretical studies

Khaef, Sepideh,Taherpour, Avat Arman,Yarie, Meysam,Zolfigol, Mohammad Ali

, p. 44946 - 44957 (2020/12/30)

Protection techniques of functional groups within the structure of organic compounds are important synthetic methods against unwanted attacks from various reagents during synthetic sequences. Acetal and thioacetal groups are well known as protective funct

House bulb light-induced photochemical acetalization of carbonyl compounds catalyzed by Eosin Y

Zhou, Quan,Jia, Tao,Li, Xiao-Xuan,Zhou, Lin,Li, Chang-Jiang,Feng, Yi-Si

supporting information, p. 1068 - 1075 (2018/05/23)

We have systematically studied the reactions of acetalization and found that high reaction efficiency can be achieved using cheap and readily available organic Eosin Y as catalyst. The reaction proceeds smoothly under house bulbs and shows excellent functional group tolerance. The substrates of the reaction system are compatible with aromatic aldehydes, aliphatic aldehydes, aromatic ketones, and cyclic ketones with high yields.

NOVEL COMPOUNDS FOR TREATING INFLAMMATORY DISEASES

-

Page/Page column 101-102, (2010/11/24)

The invention relates to novel compounds of formula (1), heteroderivatives thereof, and pharmacologically compatible salts, diastereomers, enantiomers, racemates, hydrates or solvates thereof, that are suitable for treating respiratory or gastrointestinal

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