BENZANTHRONYL

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NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C34H18O2
Molecular Weight	458.5055
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BENZANTHRONYL

Structure Search

SMILES

O=C1C2=CC=CC=C2C3=C4C1=CC=C(C4=CC=C3)C5=C6C=CC=C7C8=CC=CC=C8C(=O)C(C=C5)=C67

InChI

InChIKey=FEQOTXWZPMPKGW-UHFFFAOYSA-N

InChI=1S/C34H18O2/c35-33-27-9-3-1-7-19(27)23-11-5-13-25-21(15-17-29(33)31(23)25)22-16-18-30-32-24(12-6-14-26(22)32)20-8-2-4-10-28(20)34(30)36/h1-18H

HIDE SMILES / InChI

Molecular Formula	C34H18O2
Molecular Weight	458.5055
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Tue Apr 01 18:07:06 GMT 2025` Edited by `admin` on `Tue Apr 01 18:07:06 GMT 2025`
Record UNII	A7IH8DH3K5
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

BENZANTHRONYL

Common Name

English

NSC-13989

Preferred Name

English

4,4'-BIBENZANTHRONYL

Systematic Name

English

(4,4'-BI-7H-BENZ(DE)ANTHRACENE)-7,7'-DIONE

Common Name

English

4,4'-BIBENZANTHRONE

Systematic Name

English

DIBENZONYL

Common Name

English

4,4'-DIBENZANTHRONYL

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID6059441

Created by admin on Tue Apr 01 18:07:06 GMT 2025 , Edited by admin on Tue Apr 01 18:07:06 GMT 2025

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ECHA (EC/EINECS)

204-164-6

Created by admin on Tue Apr 01 18:07:06 GMT 2025 , Edited by admin on Tue Apr 01 18:07:06 GMT 2025

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PUBCHEM

61043

Created by admin on Tue Apr 01 18:07:06 GMT 2025 , Edited by admin on Tue Apr 01 18:07:06 GMT 2025

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NSC

13989

Created by admin on Tue Apr 01 18:07:06 GMT 2025 , Edited by admin on Tue Apr 01 18:07:06 GMT 2025

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FDA UNII

A7IH8DH3K5

Created by admin on Tue Apr 01 18:07:06 GMT 2025 , Edited by admin on Tue Apr 01 18:07:06 GMT 2025

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CAS

116-90-5

Created by admin on Tue Apr 01 18:07:06 GMT 2025 , Edited by admin on Tue Apr 01 18:07:06 GMT 2025

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