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54093-92-4

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  • Ethanol, 2,2'-[(6-chloro-4,8-di-1-piperidinylpyrimido[5,4-d]pyrimidin-2-yl)imino]bi s-

    Cas No: 54093-92-4

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54093-92-4 Usage

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6-Des(diethanolamino)-6-chloro Dipyridamole (Dipyridamole EP Impurity C) is a Dipyridamole (D492625) impurity. An antitumor nucleoside pyrimido pyrimidine.

Check Digit Verification of cas no

The CAS Registry Mumber 54093-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,9 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54093-92:
(7*5)+(6*4)+(5*0)+(4*9)+(3*3)+(2*9)+(1*2)=124
124 % 10 = 4
So 54093-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H30ClN7O2/c21-19-22-15-16(17(24-19)26-7-3-1-4-8-26)23-20(28(11-13-29)12-14-30)25-18(15)27-9-5-2-6-10-27/h29-30H,1-14H2

54093-92-4 Well-known Company Product Price

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  • (1220539)  Dipyridamole Related Compound C  United States Pharmacopeia (USP) Reference Standard

  • 54093-92-4

  • 1220539-25MG

  • 14,500.98CNY

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54093-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Des(diethanolamino)-6-chloro Dipyridamole

1.2 Other means of identification

Product number -
Other names 2-[[2-chloro-4,8-di(piperidin-1-yl)pyrimido[5,4-d]pyrimidin-6-yl]-(2-hydroxyethyl)amino]ethanol

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:54093-92-4 SDS

54093-92-4Downstream Products

54093-92-4Relevant articles and documents

PROCESSES FOR THE PREPARATION OF DIPYRIDAMOLE

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Page/Page column 19, (2011/12/14)

The present invention relates to the active pharmaceutical ingredient dipyridamole. In particular, it relates to efficient processes for the preparation of dipyridamole which are amenable to large scale commercial production and provide the required product with improved yield and purity. The present invention also relates to a novel crystallization method for the purification of dipyridamole.

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