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Home/Compounds/Research Reagent/Ethyl (2R)-2,3-epoxypropanoate
C5H8O3
116.11 g/mol
Research ReagentWarning

Ethyl (2R)-oxirane-2-carboxylate

CAS111058-33-4EC866-955-8
Category
Research Reagent
Compound Class
Ester
Primary Use
Research Compound

Ethyl (2R)-oxirane-2-carboxylate is a chiral epoxide compound featuring an ester functional group. This stereochemically defined molecule is primarily utilized as a research reagent in laboratory settings.

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

ReferenceSame Category

(E)-3,5-Dichloro-4-(3-ethoxy-2-methyl-3-oxoprop-1-en-1-yl)benzoic acid

CAS1110767-89-9

research compound

ReferenceSame Category

(S)-4-(3-(1-(Hexyloxy)ethyl)-2-methoxyphenyl)thiazol-2-amine

CAS1110767-98-0

research compound

ReferenceSame Category

Ethyl (2E)-3-[2,6-dichloro-4-[[[4-[3-[(1S)-1-(hexyloxy)ethyl]-2-methoxyphenyl]-2-thiazolyl]amino]carbonyl]phenyl]-2-methyl-2-propenoate

CAS1110768-00-7

research compound

ReferenceSame Category

3-Iodopyridin-2(1H)-one

CAS111079-46-0

research compound

Referencestereoisomer of

2-Oxiranecarboxylic acid ethyl ester

CAS111058-34-5

pharmaceutical intermediate

Referencestereoisomer of

Ethyl 2,3-epoxypropanoate

CAS4660-80-4

research compound

Safety Reference

Flammable
Flammable
Harmful
Harmful
Warning
H226Flammable liquid and vapour
H315Causes skin irritation
H317May cause an allergic skin reaction
H319Causes serious eye irritation
Identifiers
IUPAC Name

ethyl (2R)-oxirane-2-carboxylate

InChIKey

LSGWSXRILNPXKJ-SCSAIBSYSA-N

SMILES

CCOC(=O)[C@H]1CO1

Synonyms (11)
  • Ethyl (R)-(+)-Glycidate
  • ethyl 2(R)-epoxypropanoate

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