FAAH-IN-2 Gefitinib Intermediate CAS 184475-71-6 Purity >99.0% (HPLC) Factory High Quality

Chemical Name: FAAH-IN-2  CAS: 184475-71-6 Purity: >99.0% (HPLC) Appearance: Almost White to Grey Powder Intermediate of Gefitinib (CAS: 184475-35-2) High Quality, Commercial Production E-Mail: alvin@ruifuchem.com

Products Details

Chemical Properties:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement. Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of FAAH-IN-2 (CAS: 184475-71-6) with high quality, commercial production. Welcomed to order.
Item Specifications
Appearance Almost White to Grey Powder
Melting Point >260.0℃
Loss on Drying <1.00%
Related Substances
Single Impurity <1.00%
Total Impurities <1.00%
Purity / Analysis Method >99.0% (HPLC)
Test Standard Enterprise Standard
Usage Intermediate of Gefitinib (CAS: 184475-35-2)

Description:

Specifications:

Package & Storage:

Chemical Name FAAH-IN-2
Synonyms 4-(3-Chloro-4-Fluorophenylamino)-7-Methoxyquinazolin-6-ol; O-Desmorpholinopropyl Gefitinib; 4-(3-Chloro-4-Fluoroanilino)-6-Hydroxy-7-Methoxyquinazoline; Gefitinib Impurity; Gefitinib Intermediate VII
CAS Number 184475-71-6
CAT Number RF-PI1620
Stock Status In Stock 
Molecular Formula C15H11ClFN3O2
Molecular Weight 319.72 
Brand Ruifu Chemical

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Application:

FAAH-IN-2 (CAS: 184475-71-6) is an intermediate of Gefitinib (CAS: 184475-35-2), a metabolite of Gefitinib. Gefitinib is an antineoplastic target therapy drug with relatively high specificity that was developed by the British pharmaceutical company AstraZeneca; it is the first molecular targeted drug to be used in non-small cell lung cancer treatment. Epidermal growth factors (EGF) are a kind of polypeptide with a relative molecular mass of 6.45x103, and they can bind with epidermal growth factor receptors (EGFR) on target cell membrane surfaces to trigger biological effects.  EGFR is a type of tyrosine kinase (TK) type receptor, so when bound with EGF, it will promote TK activation in the receptor. This will cause tyrosine residue in the receptor to autophosphorylate and send continuous dividing signals into the cell, causing cell proliferation and differentiation. Gefitinib blocks the signal transduction pathway of cell surface EGFR to prevent tumor growth, metastasis, and growth in blood vessels, and it can induce tumor cell apoptosis.

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