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66866-66-8

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66866-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66866-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,6 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66866-66:
(7*6)+(6*6)+(5*8)+(4*6)+(3*6)+(2*6)+(1*6)=178
178 % 10 = 8
So 66866-66-8 is a valid CAS Registry Number.

66866-66-8SDS

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 phenylmethyl (4S)-4-(2-methylpropyl)-5-oxo-1,3-oxazolidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names (S)-4-isobutyl-5-oxo-oxazolidine-3-carboxylic acid benzyl ester

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:66866-66-8 SDS

66866-66-8Relevant articles and documents

A novel synthesis of N-but-3-enyl-α- and β-amino acids

Van Nguyen,Brownlee, Robert T. C.,Hughes, Andrew B.

experimental part, p. 1991 - 1998 (2010/03/24)

N-But-3-enyl-α- and β-amino acids can be prepared by cleaving 1,3-oxazolidin-5-ones and 1,3-oxazinan-6-ones in the presence of allylsilanes and boron trifluoride etherate at room temperature in good to excellent yields. Georg Thieme Verlag Stuttgart.

Microwave accelerated efficient synthesis of N-fluorenylmethoxycarbonyl/t-butoxycarbonyl/benzyloxycarbonyl-5- oxazolidinones

Tantry, Subramanyam J.,Kantharaju,Suresh Babu, Vommina V.

, p. 9461 - 9462 (2007/10/03)

The synthesis of N-protected 5-oxazolidinones using amino acids, paraformaldehyde and p-toluene sulfonic acid in a minimum amount of toluene accelerated by microwave irradiation for 3 min in high yield is described.

Selective reductions of oxazolidinones: New protocol for diastereoselective synthesis of vicinal amino alcohols

Reddy, G. Vidyasagar,Rao, G. Venkat,Iyengar

, p. 2653 - 2656 (2007/10/03)

Selective reductions of oxazolidinones using sodium borohydride and their application to the diastereoselective synthesis of vicinal amino alcohols are described.

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