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Home/Compounds/API/Voriconazole camphor sulfonate
C26H30F3N5O5S
581.6 g/mol
APIDanger

Voriconazole camphor sulfonate

CAS188416-34-4
Category
API
Compound Class
Other
Primary Use
Pharmaceutical Raw Material

Voriconazole camphor sulfonate is a salt form of the antifungal active pharmaceutical ingredient voriconazole, combined with camphor sulfonic acid. It is primarily used as a raw material in pharmaceutical manufacturing for antifungal applications.

antifungal pharmaceutical raw materialactive pharmaceutical ingredient for research

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

StrongSame Parent

Voriconazole

CAS137234-62-9

pharmaceutical raw material

StrongSame Parent

Voriconazole camphor sulfonate

CAS137234-71-0

pharmaceutical intermediate

ReferenceSame Category

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CAS188416-35-5

pharmaceutical raw material

ReferenceSame Category

Ensifentrine

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pharmaceutical raw material

ReferenceSame Category

Eptifibatide

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pharmaceutical raw material

ReferenceSame Category

(2S)-Hydroxy(phenyl)acetic acid (2R)-N-benzyl-1-(4-methoxyphenyl)propan-2-amine

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pharmaceutical raw material

Referencestereoisomer of

(2R,3R)-2-(2,4-Difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol

CAS137330-52-0

pharmaceutical raw material

Referencestereoisomer of

2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol

CAS182230-43-9

research compound

Safety Reference

Toxic
Toxic
Health Hazard
Health Hazard
Danger
H301Toxic if swallowed
H351Suspected of causing cancer
H360May damage fertility or the unborn child
Identifiers
IUPAC Name

(2R,3S)-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol;[(1R,4S)-7,7-dimethyl-2-oxo-1-bicyclo[2.2.1]heptanyl]methanesulfonic acid

InChIKey

AMYMCJHOGKVJHB-CRFUWKMFSA-N

SMILES

C[C@@H](C1=NC=NC=C1F)[C@](CN2C=NC=N2)(C3=C(C=C(C=C3)F)F)O.CC1([C@H]2CC[C@@]1(C(=O)C2)CS(=O)(=O)O)C

Synonyms (4)

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