Convenient form of anhydrous HF, stable up to 50°C. Has been used for the preparation of β-fluoroamines from amino alcohols and for the fluorination of acetylenes. Used together with hypervalent iodine(III) reagents for ipso-fluorination of para-substituted phenols providing cyclohexadienones. Employed for geminal fluorination of 2,2-diaryl-1,3-dithiolane?s. Reactant for preparation of: Epimers of shikimic acid with the features of fucosylated glycans via zinc-mediated reductive ring opening followed by a Barbier reaction Vaccinia H1-related (VHR) phosphatase inhibitor with a nonacidic phosphate-mimicking core structure Candidates for nucleic acid drugs ω-substituted gem-difluoroalkanes by oxidative desulfurization-difluorin?ation Reagent for: Halofluorination reactions.
Specifications and Purity: pyridine ~30 %, hydrogen fluoride ~70 %
MDL Number: MFCD00012436
Molecular Formula: C5H5N · (HF)x
Molecular Weight: 20.01
PubChem CID: 64774
Isomeric SMILES: C1=CC=NC=C1.F
Beilstein Registry Number: 4750150
Related Documents: https://aladdin-for-icloud-store.oss-cn-hangzhou.aliyuncs.com/aladdinsci/pdp/sds/1/H107606-SCI_e26ce728eb198900526ba56d894b7020.pdf
- UPC:
- 12352318
- Condition:
- New
- HazmatClass:
- Yes
- WeightUOM:
- LB
- MPN:
- H107606-5g
- CAS:
- 62778-11-4
- Health Hazards:
- Corrosive,Toxic
- Product Size:
- 5g
- Hazard Statement Codes:
- H300
- Precautionary Statement Codes:
- P501:P403+P233:P405:P361+P364:P305+P351+P338:P304+P340:P302+P352:P301+P330+P331:P363:P361:P330:P320:P302:P284:P280:P271:P270:P264:P262:P260
akash.verma@cenmed.com
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