1-Chlorocarbonyl-4-Piperidinopiperidine Hydrochloride CAS 143254-82-4 Irinotecan Hydrochloride Intermediate High Purity

Name: 1-Chlorocarbonyl-4-Piperidinopiperidine Hydrochloride CAS: 143254-82-4 Appearance: White or Light Yellow Powder Assay: ≥98.0% (HPLC) Intermediate of Irinotecan Hydrochloride (CAS: 100286-90-6)  High Quality, Commercial Production Inquiry: alvin@ruifuchem.com

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Chemical Properties:

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.Manufacturer Supply Irinotecan and Related Intermediates: Irinotecan Hydrochloride CAS: 100286-90-6 Irinotecan Free Base CAS: 97682-44-5 Irinotecan Hydrochloride Trihydrate CAS: 136572-09-3 7-Ethyl-10-Hydroxycamptothecin CAS: 86639-52-3  1-Chlorocarbonyl-4-Piperidinopiperidine Hydrochloride CAS: 143254-82-4
Item Specifications
Appearance White or Light Yellow Powder
Assay ≥98.0% (HPLC)
Loss on Drying ≤1.0%
Heavy Metals ≤20ppm
Test Standard Enterprise Standard
Usage Intermediate of Irinotecan Hydrochloride (CAS: 100286-90-6)

Description:

Specifications:

Package & Storage:

Chemical Name 1-Chlorocarbonyl-4-Piperidinopiperidine Hydrochloride
CAS Number 143254-82-4
CAT Number RF-PI243
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C11H20Cl2N2O
Molecular Weight 267.2
Brand Ruifu Chemical

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Application:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of 1-Chlorocarbonyl-4-Piperidinopiperidine Hydrochloride (CAS: 143254-82-4) with high quality. It is an intermediate typically in the synthesis of  Irinotecan Hydrochloride (CAS: 100286-90-6), a DNA Topoisomerase I Inhibitor.  lrinotecan hydrochloride, a semi-synthetic, water soluble derivative of the potent anticancer agent camptothecin, was launched in Japan for the treatment of lung, ovarian, and cervical cancers. lrinotecan exerts its antitumor activity via inhibition of topoisomerase I, a cellular enzyme that is involved in maintaining the topographic structure of DNA during the process of translation, transcription, and mitosis. lrinotecan undergoes de-esterification in vivo to yield an active metabolite, SN-38, which is 1000-fold more potent than the parent. Although being much less toxic than camptothecin, a significant number of patients in clinical trials exhibited side effects of leukopenia, diarrhea, nauseahromiting, and alopecia.  

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