2,3,8-TRIHYDROXY-6-METHYL-4-(1-METHYLETHYL)-1-NAPHTHALENECARBOXALDEHYDE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C15H16O4
Molecular Weight	260.2851
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 2,3,8-TRIHYDROXY-6-METHYL-4-(1-METHYLETHYL)-1-NAPHTHALENECARBOXALDEHYDE

Structure Search

SMILES

CC(C)C1=C2C=C(C)C=C(O)C2=C(C=O)C(O)=C1O

InChI

InChIKey=WWHRTLINNBKCGL-UHFFFAOYSA-N

InChI=1S/C15H16O4/c1-7(2)12-9-4-8(3)5-11(17)13(9)10(6-16)14(18)15(12)19/h4-7,17-19H,1-3H3

HIDE SMILES / InChI

Approval Year

PubMed

Title	Date	PubMed
Increased terpenoid accumulation in cotton (Gossypium hirsutum) foliage is a general wound response.	2008 Apr	18386096
Stereoselective coupling of hemigossypol to form (+)-gossypol in moco cotton is mediated by a dirigent protein.	2008 Dec	18639908

Patents

Name

Type

Language

2,3,8-TRIHYDROXY-6-METHYL-4-(1-METHYLETHYL)-1-NAPHTHALENECARBOXALDEHYDE

Systematic Name

English

ISOHEMIGOSSYPOL

Common Name

English

1-NAPHTHALENECARBOXALDEHYDE, 2,3,8-TRIHYDROXY-6-METHYL-4-(1-METHYLETHYL)-

Systematic Name

English

2,3,8-TRIHYDROXY-4-ISOPROPYL-6-METHYL-1-NAPHTHALDEHYDE

Systematic Name

English

HEMIGOSSYPOL

Common Name

English

Code System Code Type Description

CAS

40817-07-0

Created by admin on Fri Dec 15 17:58:46 GMT 2023 , Edited by admin on Fri Dec 15 17:58:46 GMT 2023

PRIMARY

EPA CompTox

DTXSID60193806

Created by admin on Fri Dec 15 17:58:46 GMT 2023 , Edited by admin on Fri Dec 15 17:58:46 GMT 2023

PRIMARY

PUBCHEM

115300

Created by admin on Fri Dec 15 17:58:46 GMT 2023 , Edited by admin on Fri Dec 15 17:58:46 GMT 2023

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FDA UNII

A7A75KAZ73

Created by admin on Fri Dec 15 17:58:46 GMT 2023 , Edited by admin on Fri Dec 15 17:58:46 GMT 2023

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SUBSTANCE RECORD


					A7A75KAZ73

2,3,8-TRIHYDROXY-6-METHYL-4-(1-METHYLETHYL)-1-NAPHTHALENECARBOXALDEHYDE