OEM/ODM Manufacturer Indacaterol Maleate Intermediate - β-D-Ribofuranose 1-Acetate 2,3,5-Tribenzoate CAS 6974-32-9 Clofarabine Intermediate High Purity – Ruifu

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OEM/ODM Manufacturer Indacaterol Maleate Intermediate - β-D-Ribofuranose 1-Acetate 2,3,5-Tribenzoate CAS 6974-32-9 Clofarabine Intermediate High Purity – Ruifu Detail:

Manufacturer with High Purity and Stable Quality
Commercial Supply Clofarabine (CAS: 123318-82-1) Related Intermediates:
Clofarabine CAS: 123318-82-1
2-Deoxy-2-fluoro-1,3,5-tri-O-benzoyl-α-D-arabinofuranose CAS: 97614-43-2
β-D-Ribofuranose 1-Acetate 2,3,5-Tribenzoate CAS: 6974-32-9
2,6-Dichloropurine CAS: 5451-40-1

Chemical Name	β-D-Ribofuranose 1-Acetate 2,3,5-Tribenzoate
Synonyms	1-O-Acetyl-2,3,5-tri-O-benzoyl-β-D-Ribofuranose
CAS Number	6974-32-9
CAT Number	RF-PI222
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	C28H24O9
Molecular Weight	504.49
Brand	Ruifu Chemical

Item	Specifications
Appearance	White or Off-White Crystalline Powder
Assay / Analysis Method	≥98.0% (HPLC)
Melting Point	126.0~133.0℃
Loss on Drying	≤0.50%
Residue on Ignition	≤0.50%
Heavy Metals	≤20ppm
Test Standard	Enterprise Standard
Usage	Pharmaceutical Intermediate of Clofarabine CAS: 123318-82-1

Package: Bottle, Aluminum foil bag, Cardboard drum, 25kg/Drum, or according to customer’s requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

β-D-Ribofuranose 1-Acetate 2,3,5-Tribenzoate CAS 6974-32-9 is an inhibitor of neutrophil-keyhole limpet hemocyanin adhesion. Anti-inflammatory agent. Azacitidine Related Compound B.

Clofarabine (CAS: 123318-82-1) is a novel purine nucleoside anticancer drugs is first successfully developed by the Top10 biopharmaceutical company of the United States—Genzyme Corporation, NASDAQ: GENZ) with the trade names being “Clofarabine”. On December 28, 2004 the US food and Drug Administration (FDA) used fast-track for approval of clofarabine for application to children with refractory or relapsed acute lymphocytic leukemia. It is currently the only available drugs for the special treatment of children with acute myelogenous leukemia (ALL); it has an excellent efficacy on the treatment of leukemia with well tolerance and no unpredictable adverse reactions. It can be administrated through either administered intravenously or administered orally. This drug is the first product approved for being dedicated to the treatment of the children’s leukemia in more than ten years.

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