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89053-48-5

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89053-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89053-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,5 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89053-48:
(7*8)+(6*9)+(5*0)+(4*5)+(3*3)+(2*4)+(1*8)=155
155 % 10 = 5
So 89053-48-5 is a valid CAS Registry Number.

89053-48-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-3-methyl-5-phenyloxazolidin-4-one

1.2 Other means of identification

Product number -
Other names 3-Methyl-5-phenyl-oxazolidin-4-one

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:89053-48-5 SDS

89053-48-5Downstream Products

89053-48-5Relevant articles and documents

Enantioselective photoreaction in inclusion crystal

Miyamoto, Hisakazu,Kikuchi, Siro,Oki, Yasuo,Inoue, Mitsuhiro,Kanemoto, Kazuyuki,Toda, Fumio

, p. 73 - 78 (2007/10/03)

Mixing of powdered chiral hosts and achiral guest compounds gives inclusion complexes in which the latter molecules are arranged in a chiral form. Freezing of the chirality of the guest compounds by photoirradiation in the solid state gives optically active photoreaction products.

OPTICAL ACTIVITY OF LACTONES AND LACTAMS-II CHIROPTICAL PROPERTIES OF 4-OXAZOLIDINONES

Polonski, T.

, p. 3139 - 3143 (2007/10/02)

Several optically active 4-oxazolidinones were obtained from amides or N-methylamides of corresponding α-hydroxy acids.The influence of solvent and substituent on their CD was studied.The predominance of the envelpe conformation was established for these compounds, the degree of puckering being enhanced by polar solvents.The folded form with the aromatic ring facing the oxazolidinone ring was observed for 5-benzyl substituted oxazolidinone derivatives.

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