Chalcone Oxide, rel-trans-

Details

Stereochemistry	RACEMIC
Molecular Formula	C15H12O2
Molecular Weight	224.2546
Optical Activity	( + / - )
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

O=C([C@@H]1O[C@H]1C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=UQGMJZQVDNZRKT-GJZGRUSLSA-N

InChI=1S/C15H12O2/c16-13(11-7-3-1-4-8-11)15-14(17-15)12-9-5-2-6-10-12/h1-10,14-15H/t14-,15-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C15H12O2
Molecular Weight	224.2546
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:16:04 GMT 2025` Edited by `admin` on `Mon Mar 31 22:16:04 GMT 2025`
Record UNII	U2AKU44C26
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-402160

Preferred Name

English

Chalcone Oxide, rel-trans-

Common Name

English

CHALCONE OXIDE

Systematic Name

English

trans-1,3-Diphenyl-2,3-epoxyprop-1-one

Systematic Name

English

rel-Phenyl[(2R,3S)-3-phenyloxiranyl]methanone

Systematic Name

English

rel-trans-Chalcone Oxide

Common Name

English

Methanone, phenyl(3-phenyloxiranyl)-, trans-

Systematic Name

English

2-Benzoyl-3-phenyloxirane, trans-

Common Name

English

trans-1,3-Diphenyl-1,2-epoxy-3-propanone

Systematic Name

English

trans-2-Benzoyl-3-phenyloxirane

Systematic Name

English

Methanone, phenyl[(2R,3S)-3-phenyl-2-oxiranyl]-, rel-

Systematic Name

English

Methanone, phenyl[(2R,3S)-3-phenyloxiranyl]-, rel-

Systematic Name

English

Code System Code Type Description

NSC

402160

Created by admin on Mon Mar 31 22:16:04 GMT 2025 , Edited by admin on Mon Mar 31 22:16:04 GMT 2025

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FDA UNII

U2AKU44C26

Created by admin on Mon Mar 31 22:16:04 GMT 2025 , Edited by admin on Mon Mar 31 22:16:04 GMT 2025

PRIMARY

CAS

7570-86-7

Created by admin on Mon Mar 31 22:16:04 GMT 2025 , Edited by admin on Mon Mar 31 22:16:04 GMT 2025

PRIMARY

EPA CompTox

DTXSID601032735

Created by admin on Mon Mar 31 22:16:04 GMT 2025 , Edited by admin on Mon Mar 31 22:16:04 GMT 2025

PRIMARY

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