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121485-54-9

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121485-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121485-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,8 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121485-54:
(8*1)+(7*2)+(6*1)+(5*4)+(4*8)+(3*5)+(2*5)+(1*4)=109
109 % 10 = 9
So 121485-54-9 is a valid CAS Registry Number.

121485-54-9SDS

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 4-ethenyl-N,3-diphenyl-1,3-oxazolidin-2-imine

1.2 Other means of identification

Product number -
Other names N-phenyl-3-phenyl-4-vinyl-1,3-oxazolidin-2-imine

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:121485-54-9 SDS

121485-54-9Downstream Products

121485-54-9Relevant articles and documents

A correlation study of bisphosphine ligand bite angles with enantioselectivity in Pd-catalyzed asymmetric transformations

Raghunath, Malati,Zhang, Xumu

, p. 8213 - 8216 (2005)

Among the bisphosphine ligands, we have previously developed C n-TunePhos (n = 1-6) as a family of ligands with tunable bite angles. The increase in spacer -CH2- groups in this family of ligands causes changes in ligand dihedral angl

Selective α-Cleavage Cycloaddition of Oxiranes with Heterocumulenes Catalyzed by Tetraphenylstibonium Iodide

Fujiwara, Masahiro,Baba, Akio,Matsuda, Haruo

, p. 1351 - 1357 (2007/10/02)

A catalytic amount of tetraphenylstibonium iodide (1) promoted unusual cycloadditions of oxiranes with isocyanates or carbodiimides, forming 3,4-disubstituted oxazolidin-2-ones 2 and oxazolidin-2-imines 4 under very mild conditions, respectively.In partic

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