TERT-BUTYL GLYCIDYL ETHER

Details

Stereochemistry	RACEMIC
Molecular Formula	C7H14O2
Molecular Weight	130.1849
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

CC(C)(C)OCC1CO1

InChI

InChIKey=SFJRUJUEMVAZLM-UHFFFAOYSA-N

InChI=1S/C7H14O2/c1-7(2,3)9-5-6-4-8-6/h6H,4-5H2,1-3H3

HIDE SMILES / InChI

Molecular Formula	C7H14O2
Molecular Weight	130.1849
Charge	0
Count	MOL RATIO 1 MOL RATIO (average)

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

PubMed

Show entries

Title	Date	PubMed
Novel microbial epoxide hydrolases for biohydrolysis of glycidyl derivatives.	2005 Dec 6	16061300
Purification and characterisation of a novel enantioselective epoxide hydrolase from Aspergillus niger M200.	2006 Feb	16343776
Cloning of an epoxide hydrolase-encoding gene from Aspergillus niger M200, overexpression in E. coli, and modification of activity and enantioselectivity of the enzyme by protein engineering.	2007 Oct 15	17875334

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Patents

Substance Class	Chemical
Record UNII	35F8X83D0G
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

P-TERT-BUTYL GLYCIDYL ETHER

Preferred Name

English

TERT-BUTYL GLYCIDYL ETHER

Systematic Name

English

1-TERT-BUTOXY-2,3-EPOXYPROPANE

Systematic Name

English

TERT-BUTYL GLYCIDYL ETHER, (±)-

Systematic Name

English

2,3-EPOXYPROPYL-TERT-BUTYL ETHER

Systematic Name

English

Showing 1 to 5 of 16 entries

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Code System

Code

Type

Description

EPA CompTox

DTXSID4024692

PRIMARY

PUBCHEM

24314

PRIMARY

FDA UNII

35F8X83D0G

PRIMARY

ECHA (EC/EINECS)

231-640-0

PRIMARY

CAS

7665-72-7

PRIMARY

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Related Record

Type

Details


					O65YZ0RP4G

TERT-BUTYL GLYCIDYL ETHER, (-)-

ENANTIOMER -> RACEMATE


					G28UV61J7C

TERT-BUTYL GLYCIDYL ETHER, (+)-

ENANTIOMER -> RACEMATE

Showing 1 to 2 of 2 entries

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