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150884-56-3

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150884-56-3 Usage

Chemical Properties

white to very slightly beige crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 150884-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,8,8 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150884-56:
(8*1)+(7*5)+(6*0)+(5*8)+(4*8)+(3*4)+(2*5)+(1*6)=143
143 % 10 = 3
So 150884-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O3/c1-13(2,3)17-12(16)15-11(18-15)10-6-4-9(8-14)5-7-10/h4-7,11H,1-3H3/t11-,15?/m1/s1

150884-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-BOC-3-(4-Cyanophenyl)oxaziridine

1.2 Other means of identification

Product number -
Other names tert-butyl 3-(4-cyanophenyl)oxaziridine-2-carboxylate

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:150884-56-3 SDS

150884-56-3Relevant articles and documents

PYRAZOLE AMIDE DERIVATIVE

-

, (2015/09/28)

The present invention relates to a novel compound having a function of inhibiting RORγ activity. The present invention also relates to pharmaceutical composition comprising the compound, a use of the compound in treating or preventing autoimmune diseases, inflammatory diseases, metabolic diseases, or cancer diseases.

Electrophilic Amination: Preparation and Use of N-Boc-3-(4-cyanophenyl)oxaziridine, a New Reagent That Transfers a N-Boc Group to N- and C-Nucleophiles

Vidal, Joelle,Guy, Laure,Sterin, Sebastien,Collet, Andre

, p. 4791 - 4793 (2007/10/02)

We describe the preparation of the title compound 2b via aza-Wittig reaction of N-Boc-triphenyliminophosphorane (6) with 4-cyanobenzaldehyde followed by Oxone oxidation of the resulting imine 5b.Oxaziridine 2b is a stable, crystalline solid, which transfers under mild conditions its N-Boc fragment to primary and secondary amines (to give Nβ-Boc-hydrazines) and enolates (to give N-Boc-amino drivatives).

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