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32278-16-3

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32278-16-3 Usage

General Description

3-(tert-butyl)-3,4-dihydro-2H-1,4-benzoxazine is a chemical compound with the molecular formula C12H17NO. It is a heterocyclic compound containing a benzoxazine ring, a cyclic ether with a nitrogen atom. 3-(TERT-BUTYL)-3,4-DIHYDRO-2H-1,4-BENZOXAZINE is commonly used as a monomer in the production of thermosetting polymers, particularly as a component in epoxy resins. It is known for its high heat resistance, flame retardancy, and electrical insulation properties, making it valuable in a variety of industrial applications such as adhesives, coatings, and electronic materials. Additionally, it has been studied for its potential use in biomedical materials due to its biocompatibility and resistance to enzyme degradation.

Check Digit Verification of cas no

The CAS Registry Mumber 32278-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,7 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32278-16:
(7*3)+(6*2)+(5*2)+(4*7)+(3*8)+(2*1)+(1*6)=103
103 % 10 = 3
So 32278-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-12(2,3)11-8-14-10-7-5-4-6-9(10)13-11/h4-7,11,13H,8H2,1-3H3/t11-/m0/s1

32278-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-tert-butyl-3,4-dihydro-2H-1,4-benzoxazine

1.2 Other means of identification

Product number -
Other names 3-tert-butyl-3,4-dihydro-2H-benzo[1,4]oxazine

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:32278-16-3 SDS

32278-16-3Downstream Products

32278-16-3Relevant articles and documents

N-tosyl-(S)-prolyl chloride in kinetic resolution of racemic heterocyclic amines

Gruzdev,Vakarov,Levit,Krasnov

, p. 1795 - 1807 (2014/05/06)

The kinetic resolution of racemic heterocyclic amines via acylation with N-tosyl-(S)-prolyl chloride was systematically investigated. It was established that racemic mixtures of aromatic amines could be resolved with high efficiency, while the acylation of 2- and 3-methylpiperidines occurred with low diastereoselectivity. A method for the preparation of enantiomerically pure (3R)-7,8-difluoro-3-methyl-3,4-dihydro-2H-[1,4]benzoxazine was developed.

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