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13213-90-6

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13213-90-6 Usage

Chemical class

Organic compounds known as benzoxazines.

Physical appearance

Pale yellow or orange crystalline solid.

Biological activities

Anti-fungal, anti-bacterial, anti-viral, and anti-cancer properties.

Industrial uses

Synthesis of pharmaceuticals and agrochemicals.

Potential applications

Development of organic semiconductors and optical brighteners in materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 13213-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,1 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13213-90:
(7*1)+(6*3)+(5*2)+(4*1)+(3*3)+(2*9)+(1*0)=66
66 % 10 = 6
So 13213-90-6 is a valid CAS Registry Number.

13213-90-6SDS

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 1-phenyl-4H-3,1-benzoxazin-2-one

1.2 Other means of identification

Product number -
Other names 1,4-Dihydro-1-phenyl-2H-3,1-benzoxazin-2-one

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:13213-90-6 SDS

13213-90-6Downstream Products

13213-90-6Relevant articles and documents

Sunlight-Driven Forging of Amide/Ester Bonds from Three Independent Components: An Approach to Carbamates

Zhao, Yating,Huang, Binbin,Yang, Chao,Chen, Qingqing,Xia, Wujiong

, p. 5572 - 5575 (2016/11/17)

A photoredox catalytic route to carbamates enabled by visible irradiation (or simply sunlight) has been developed. This process leads to a novel approach to the construction of heterocyclic rings wherein the amide or ester motifs of carbamates were assembled from three isolated components. Large-scale experiments were realized by employing continuous flow techniques, and reuse of photocatalyst demonstrated the green and sustainable aspects of this method.

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