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Fosaprepitant (CAS No.: 172673-20-0)

Manus Aktteva Biopharma LLP is an ISO 9001:2015 Certified Global Supplier based in India for the product Fosaprepitant, 172673-20-0.
We offer the product Fosaprepitant, 172673-20-0 from our manufacturer / supplier / principals for your Research and Development / Evaluation or Commercial requirements, based on the product's availability from our network. We can also offer Fosaprepitant, 172673-20-0 intermediates with the supportive technical package required for evaluation.
We respect our customer's requirements of strict regulatory compliance and specification needs by offering the API - Active Pharmaceutical Ingredients and intermediates transparently while offering easy access to manufacturer / supplier / principals with affordable and high-quality raw materials.
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CAS number:

172673-20-0

Chemical Name:

[3-[[(2R,3S)-2-[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]-3-(4-fluorophenyl)-4-morpholinyl]methyl]-2,5-dihydro-5-oxo-1H-1,2,4-triazol-1-yl]phosphonic acid, Fosaprepitant (CAS No.: 172673-20-0)

Manufacturer Certificate:

cGMP, WHO GMP, USFDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

[3-[[(2R,3S)-2-[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]-3-(4-fluorophenyl)-4-morpholinyl]methyl]-2,5-dihydro-5-oxo-1H-1,2,4-triazol-1-yl]phosphonic acid, Fosaprepitant (CAS No.: 172673-20-0)

Molecular Formula

C23H22F7N4O6P

Molecular Weight

614.41

Manufacturer Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Availability

FOR R&D PURPOSE

Product Name	CAS No.
Tetra benzyl pyrophosphate	990-91-0	View \| Inquire

Manufacturer Documentation / Approvals :

USDMF	EDMF	MHRA - UK

Products protected by valid patents from a manufacturer are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use from a manufacturer in accordance with 35 USC 271 +A13(1)
Products falling in to controlled substance category / list of schedule drugs shall be exported directly from the manufacturer principals only against receipt of original import permission issued by concerned authorities of the importing country.
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