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104320-68-5

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104320-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104320-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,2 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104320-68:
(8*1)+(7*0)+(6*4)+(5*3)+(4*2)+(3*0)+(2*6)+(1*8)=75
75 % 10 = 5
So 104320-68-5 is a valid CAS Registry Number.

104320-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-4-(methoxycarbonyl)-5-phenyl-2-oxazoline

1.2 Other means of identification

Product number -
Other names 2-Oxazolin-4-carbonsaeure-methylester

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:104320-68-5 SDS

104320-68-5Relevant articles and documents

Homogeneous Catalysis with Dicationic Pd(II) Complexes: Aldol Reaction of Methyl Isocyanoacetate with Benzaldehyde

Nesper, Reinhard,Pregosin, Paul S.,Puentener, Kurt,Woerle, Michael

, p. 2239 - 2249 (1993)

A series of dicationic Pd(II)-acetonitrile complexes containing bi- and tridentate nitrogen and bidentate phosphine ligands (some of which are chiral) has been prepared as their BF4 salts.The molecular structures for two of these, (BF4)2

Enantioselective Synthesis: Steric and Electronic Effects of the Substrates upon Stereoselectivity in the Gold(I)-Catalyzed Aldol Reaction with Chiral Ferrocenylamine Ligands

Togni, Antonio,Pastor, Stephen D.

, p. 1038 - 1042 (1989)

Enantioselectivity in the gold(I)-catalyzed aldol reaction with chiral ferrocenylamine ligands is strongly dependent upon both the steric and electronic effects of the substrates.In the reaction of pyridine-2-, 3-, and 4-carbaldehydes with ethyl 2-isocyan

Catalytic Asymmetric Aldol Reaction: Reaction of Aldehydes with Isocyanoacetate Catalyzed by a Chiral Ferrocenylphosphine-Gold(I) Complex

Ito, Yoshihiko,Sawamura, Masaya,Hayashi, Tamio

, p. 6405 - 6406 (1986)

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Highly active copper-network catalyst for the direct aldol reaction

Ohta, Hidetoshi,Uozumi, Yasuhiro,Yamada, Yoichi M. A.

supporting information; experimental part, p. 2545 - 2549 (2012/06/18)

The development of a highly active solid-phase catechol-copper network catalyst for direct aldol reaction is described. The catalyst was prepared from an alkyl-chain-linked bis(catechol) and a copper(II) complex. The direct aldol reaction between carbonyl

A new family of cinchona-derived amino phosphine precatalysts: Application to the highly enantio- and diastereoselective silver-catalyzed isocyanoacetate aldol reaction

Sladojevich, Filippo,Trabocchi, Andrea,Guarna, Antonio,Dixon, Darren J.

supporting information; experimental part, p. 1710 - 1713 (2011/04/15)

A new class of readily accessible chiral amino-phosphine precatalysts derived from 9-amino(9-deoxy) epicinchona alkaloids has been developed. In combination with Ag(I) salts, these amino-phosphines performed as effective cooperative Brnsted base/Lewis aci

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