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3-hydroxy-9-phenyl-8-oxa-10-azabicyclo[4.4.0]deca-2,4,9,11-tetraen-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85915-62-4

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85915-62-4 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 25, p. 715, 1988 DOI: 10.1002/jhet.5570250303

Check Digit Verification of cas no

The CAS Registry Mumber 85915-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,1 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85915-62:
(7*8)+(6*5)+(5*9)+(4*1)+(3*5)+(2*6)+(1*2)=164
164 % 10 = 4
So 85915-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H9NO3/c16-10-6-7-11-12(8-10)15-13(18-14(11)17)9-4-2-1-3-5-9/h1-8,16H

85915-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-hydroxy-2-phenyl-3,1-benzoxazin-4-one

1.2 Other means of identification

Product number -
Other names 7-hydroxy-2-phenyl-[3,1]benzoxazin-4-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:85915-62-4 SDS

85915-62-4Relevant academic research and scientific papers

The Phytoalexins of Oat Leaves: 4H-3,1-Benzoxazin-4-ones or Amides?

Crombie, Leslie,Mistry, Jayshree

, p. 2647 - 2648 (2007/10/02)

Synthetic evidence is presented that the major phytoalexin of oat leaves is not the 4H-3,1-benzoxazin-4-one previously reported, but the corresponding amide.Other oat and carnation phytoalexins are prepared.

Novel synthesis of dianthalexin (Phytoalexin) analogues preparation

Hauteville,Ponchet,Ricci,Favre-Bonvin

, p. 715 - 718 (2007/10/02)

Two phytoalexins, previously isolated from carnation infected by Phytophthora parasitica D., were synthesized: 2-phenyl-7-hydroxy-4H-3,l-benzoxazin-4-one (Dianthalexin) and 2-(2-hydroxybenzoyl)-amino-4-methoxybenzoic acid (Dianthramide A). The first one w

DIANTHALEXINE, NOUVELLE PHYTOALEXINE, DE TYPE BENZOXAZINONE, ISOLEE DE L'OEILLET DIANTHUS CARYOPHYLLUS L. (CARYOPHYLLACEES).

Bouillant, Marie-Louise,Favre-Bonvin, Jean,Ricci, Pierre

, p. 51 - 52 (2007/10/02)

The major phytoalexin from carnation has been identified as 7-hydroxy 2-phenyl 4H-3, 1-benzoxazin-4-one, and named dianthalexin (1).

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