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Details

Stereochemistry RACEMIC
Molecular Formula C13H18O2
Molecular Weight 206.2808
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-TERT-BUTYLPHENYL GLYCIDYL ETHER

SMILES

CC(C)(C)C1=CC=C(OCC2CO2)C=C1

InChI

InChIKey=HHRACYLRBOUBKM-UHFFFAOYSA-N
InChI=1S/C13H18O2/c1-13(2,3)10-4-6-11(7-5-10)14-8-12-9-15-12/h4-7,12H,8-9H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C13H18O2
Molecular Weight 206.2808
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
An attempt to improve diagnostics of contact allergy due to epoxy resin systems. First results of the multicentre study EPOX 2002.
2004 Nov-Dec
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:26:49 GMT 2023
Edited
by admin
on Sat Dec 16 10:26:49 GMT 2023
Record UNII
DUA9665YBG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-TERT-BUTYLPHENYL GLYCIDYL ETHER
Systematic Name English
3-(4-TERT-BUTYLPHENOXY)-1,2-EPOXYPROPANE
Systematic Name English
P-TERT-BUTYLPHENOL GLYCIDYL ETHER
Common Name English
TERT-BUTYL PHENYL GLYCIDYL ETHER
Systematic Name English
1-(P-TERT-BUTYLPHENOXY)-2,3-EPOXYPROPANE
Common Name English
GLYCIDYL 4-TERT-BUTYLPHENYL ETHER
Systematic Name English
OXIRANE, ((4-(1,1-DIMETHYLETHYL)PHENOXY)METHYL)-
Systematic Name English
(4-TERT-BUTYLPHENOXY)METHYLOXIRANE
Systematic Name English
2-((4-TERT-BUTYLPHENOXY)METHYL)OXIRANE
Systematic Name English
OXIRANE, 2-((4-(1,1-DIMETHYLETHYL)PHENOXY)METHYL)-
Systematic Name English
GLYCIDYL P-TERT-BUTYLPHENYL ETHER
Common Name English
PROPANE, 1-(P-TERT-BUTYLPHENOXY)-2,3-EPOXY-
Common Name English
P-TERT-BUTYLPHENYL GLYCIDYL ETHER
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
221-453-2
Created by admin on Sat Dec 16 10:26:50 GMT 2023 , Edited by admin on Sat Dec 16 10:26:50 GMT 2023
PRIMARY
PUBCHEM
18360
Created by admin on Sat Dec 16 10:26:50 GMT 2023 , Edited by admin on Sat Dec 16 10:26:50 GMT 2023
PRIMARY
CAS
3101-60-8
Created by admin on Sat Dec 16 10:26:50 GMT 2023 , Edited by admin on Sat Dec 16 10:26:50 GMT 2023
PRIMARY
EVMPD
SUB169864
Created by admin on Sat Dec 16 10:26:50 GMT 2023 , Edited by admin on Sat Dec 16 10:26:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID1024702
Created by admin on Sat Dec 16 10:26:50 GMT 2023 , Edited by admin on Sat Dec 16 10:26:50 GMT 2023
PRIMARY
FDA UNII
DUA9665YBG
Created by admin on Sat Dec 16 10:26:50 GMT 2023 , Edited by admin on Sat Dec 16 10:26:50 GMT 2023
PRIMARY
SMS_ID
100000159577
Created by admin on Sat Dec 16 10:26:50 GMT 2023 , Edited by admin on Sat Dec 16 10:26:50 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE