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Home/Compounds/Other/(2S)-(+)-Glycidyl tosylate
C10H12O4S
228.27 g/mol
OtherDanger

(S)-Glycidyl tosylate

CAS70987-78-9EC417-210-7
Category
Other
Compound Class
n.a
Primary Use
Research reagent

(S)-Glycidyl tosylate is an organic compound featuring an epoxide ring and a tosylate ester group. It is commonly used as a chiral building block in organic synthesis, particularly for introducing epoxide functionality in stereoselective reactions.

Chiral building block in organic synthesisReagent for introducing epoxide functionality

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

SimilarStructure SimilarSimilarity 0.76

(S)-Oxetan-2-ylmethyl 4-methylbenzenesulfonate

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chemical intermediate for research

ReferenceSame Category

5-(4-Nitrophenyl)-2-furaldehyde

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research chemical intermediate

ReferenceSame Category

3-Hydroxy-2,6-pyridinedicarboxylic acid

CAS71502-30-2

research reagent

ReferenceSame Category

Ethyl isobutyrylacetate

CAS7152-15-0

Chemical intermediate

Referencestereoisomer of

(R)-glycidyl tosylate

CAS113826-06-5

pharmaceutical intermediate

Referencesame scaffold

(S)-(+)-Glycidyl-4-nitrobenzenesulfonate

CAS118712-60-0

pharmaceutical intermediate

Referencesame scaffold

(S)-(+)-Glycidyl nosylate

CAS115314-14-2

pharmaceutical intermediate

Safety Reference

Corrosive
Corrosive
Harmful
Harmful
Health Hazard
Health Hazard
Environmental Hazard
Environmental Hazard
Danger
H317May cause an allergic skin reaction
H318Causes serious eye damage
H341Suspected of causing genetic defects
H350May cause cancer
H411Toxic to aquatic life with long lasting effects

Customs Tariff Classification

The international HS code for (S)-Glycidyl tosylate (CAS 70987-78-9) is 2910.90.

HS code (international, 6-digit)

2910.90

EU CN code (8-digit)

2910 90 00

Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.

Identifiers
IUPAC Name

[(2S)-oxiran-2-yl]methyl 4-methylbenzenesulfonate

InChIKey

NOQXXYIGRPAZJC-VIFPVBQESA-N

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OC[C@@H]2CO2

Synonyms (21)
  • (+)-Glycidyl tosylate
  • (2S)-(+)-Glycidyl tosylate
  • (S)-Glycidyl tosylate
  • Glycidyl tosylate, (S)-

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