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Details

Stereochemistry RACEMIC
Molecular Formula C5H8O3
Molecular Weight 116.1152
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-Butylene carbonate, trans-

SMILES

C[C@@H]1OC(=O)O[C@H]1C

InChI

InChIKey=LWLOKSXSAUHTJO-IMJSIDKUSA-N
InChI=1S/C5H8O3/c1-3-4(2)8-5(6)7-3/h3-4H,1-2H3/t3-,4-/m0/s1

HIDE SMILES / InChI

Molecular Formula C5H8O3
Molecular Weight 116.1152
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 Sat Dec 16 19:14:30 GMT 2023
Edited
by admin
on Sat Dec 16 19:14:30 GMT 2023
Record UNII
V4U69J5MK2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3-Butylene carbonate, trans-
Systematic Name English
1,3-Dioxolan-2-one, 4,5-dimethyl-, (4R,5R)-rel-
Systematic Name English
trans-2,3-Butylene carbonate
Systematic Name English
rel-(4R,5R)-4,5-Dimethyl-1,3-dioxolan-2-one
Systematic Name English
1,3-Dioxolan-2-one, 4,5-dimethyl-, trans-
Systematic Name English
trans-4,5-Dimethyl-1,3-dioxolan-2-one
Systematic Name English
Code System Code Type Description
CAS
65941-76-6
Created by admin on Sat Dec 16 19:14:30 GMT 2023 , Edited by admin on Sat Dec 16 19:14:30 GMT 2023
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WIKIPEDIA
trans-2,3-Butylene carbonate
Created by admin on Sat Dec 16 19:14:30 GMT 2023 , Edited by admin on Sat Dec 16 19:14:30 GMT 2023
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PUBCHEM
10080377
Created by admin on Sat Dec 16 19:14:30 GMT 2023 , Edited by admin on Sat Dec 16 19:14:30 GMT 2023
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FDA UNII
V4U69J5MK2
Created by admin on Sat Dec 16 19:14:30 GMT 2023 , Edited by admin on Sat Dec 16 19:14:30 GMT 2023
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Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE