5-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-7-ol, (2S)-

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C16H16O3
Molecular Weight	256.2964
Optical Activity	( - )
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 5-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-7-ol, (2S)-

Structure Search

SMILES

COC1=C2CC[C@H](OC2=CC(O)=C1)C3=CC=CC=C3

InChI

InChIKey=UNCVBXFEZHBZKN-AWEZNQCLSA-N

InChI=1S/C16H16O3/c1-18-15-9-12(17)10-16-13(15)7-8-14(19-16)11-5-3-2-4-6-11/h2-6,9-10,14,17H,7-8H2,1H3/t14-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C16H16O3
Molecular Weight	256.2964
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Wed Apr 02 06:26:18 GMT 2025` Edited by `admin` on `Wed Apr 02 06:26:18 GMT 2025`
Record UNII	6TGX2B7YLF
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

5-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-7-ol, (2S)-

Systematic Name

English

(2S)-5-Methoxy-7-flavanol

Preferred Name

English

2H-1-Benzopyran-7-ol, 3,4-dihydro-5-methoxy-2-phenyl-, (S)-

Systematic Name

English

(2s)-5-Methoxyflavan-7-ol

Common Name

English

7-Hydroxy-5-methoxyflavan

Common Name

English

2H-1-Benzopyran-7-ol, 3,4-dihydro-5-methoxy-2-phenyl-, (2S)-

Systematic Name

English

(2S)-5-Methoxy-2-phenyl-3,4-dihydro-2H-chromen-7-ol

Systematic Name

English

(2S)-3,4-Dihydro-5-methoxy-2-phenyl-2H-1-benzopyran-7-ol

Systematic Name

English

Code System Code Type Description

FDA UNII

6TGX2B7YLF

Created by admin on Wed Apr 02 06:26:18 GMT 2025 , Edited by admin on Wed Apr 02 06:26:18 GMT 2025

PRIMARY

PUBCHEM

14885875

Created by admin on Wed Apr 02 06:26:18 GMT 2025 , Edited by admin on Wed Apr 02 06:26:18 GMT 2025

PRIMARY

EPA CompTox

DTXSID501236413

Created by admin on Wed Apr 02 06:26:18 GMT 2025 , Edited by admin on Wed Apr 02 06:26:18 GMT 2025

PRIMARY

CAS

35290-20-1

Created by admin on Wed Apr 02 06:26:18 GMT 2025 , Edited by admin on Wed Apr 02 06:26:18 GMT 2025

PRIMARY