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90332-63-1

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  • Benzenepropanoic acid, b-(benzoylamino)-a-hydroxy-,(2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-6,11-dihydroxy-4a,8,13,13-tetrameth

    Cas No: 90332-63-1

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90332-63-1 Usage

Chemical Properties

Off-White Solid

Uses

Different sources of media describe the Uses of 90332-63-1 differently. You can refer to the following data:
1. A metabolite of Paclitaxel (P132500). Paclitaxel - In House Impurity.
2. A metabolite of Paclitaxel (P132500).

Check Digit Verification of cas no

The CAS Registry Mumber 90332-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,3 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90332-63:
(7*9)+(6*0)+(5*3)+(4*3)+(3*2)+(2*6)+(1*3)=111
111 % 10 = 1
So 90332-63-1 is a valid CAS Registry Number.

90332-63-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Xylosyl-10-deacetyltaxol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90332-63-1 SDS

90332-63-1Upstream product

90332-63-1Downstream Products

90332-63-1Relevant articles and documents

Preparation method of 7-xylosyltaxol

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Paragraph 0015; 0030; 0032; 0039; 0041; 0044; 0046, (2021/09/08)

The invention relates to a preparation method of 7-xylosyltaxol, and belongs to the technical field of preparation of taxane anticancer drugs, the preparation method comprises the following steps: S1, dissolving a 7-xylosyl-10-deacetylpaclitaxel extract with dichloromethane and pyridine, dropwise adding 2,2,2-trichloroethyl chloroformate while stirring, and reacting to obtain a product I; S2, dissolving the product I in methanol and acetic acid, adding zinc powder, and stirring for reaction to obtain a product II; S3, dissolving the product II in tetrahydrofuran, adding cerium trichloride, dropwise adding acetic anhydride, and stirring for reaction to obtain a product III; and S4, dissolving the product III in methanol, adding a 30% dimethylamine methanol solution, and carrying out a stirring reaction to obtain the 7-xylosyltaxol. The method has the advantages of accessibility of initial materials, mild reaction conditions and high purity of target products, and can be used for large-scale preparation.

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