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22887-57-6

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22887-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22887-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,8 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22887-57:
(7*2)+(6*2)+(5*8)+(4*8)+(3*7)+(2*5)+(1*7)=136
136 % 10 = 6
So 22887-57-6 is a valid CAS Registry Number.

22887-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-p-Chlorophenyl-4-phenyl-2-oxazolin-5-one

1.2 Other means of identification

Product number -
Other names 2-p-Chlorphenyl-4-phenyl-oxazolin-5-on

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:22887-57-6 SDS

22887-57-6Relevant articles and documents

Enantioselective iridium catalyzed α-alkylation of azlactones by a tandem asymmetric allylic alkylation/aza-Cope rearrangement

Bai, Xue-Dan,Zhang, Qing-Feng,He, Ying

, p. 5547 - 5550 (2019/05/21)

The development of an iridium catalyzed enantioselective α-alkylation of azlactones has been described. The reaction provides rapid access to a wide range of enantio-enriched quaternary carbon center allylated 2,4-diaryloxazol-5(2H)-ones in excellent yiel

Dynamic kinetic resolution of azlactones catalyzed by chiral Bronsted acids

Lu, Guojian,Birman, Vladimir B.

supporting information; body text, p. 356 - 358 (2011/03/22)

Chiral Bronsted acids have been shown for the first time to catalyze the dynamic kinetic resolution of azlactones. 3,3'-Bis-(9-anthryl)-BINOL phosphoric acid 3c is particularly effective in the case of 4-aryl-substituted substrates, producing 85-92% ee's.

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