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N(4)-succinyl-1-beta-D-arabinofuranosylcytosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55726-37-9

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55726-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55726-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,2 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55726-37:
(7*5)+(6*5)+(5*7)+(4*2)+(3*6)+(2*3)+(1*7)=139
139 % 10 = 9
So 55726-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H17N3O8/c17-5-6-10(21)11(22)12(24-6)16-4-3-7(15-13(16)23)14-8(18)1-2-9(19)20/h3-4,6,10-12,17,21-22H,1-2,5H2,(H,19,20)(H,14,15,18,23)/t6-,10-,11+,12-/m1/s1

55726-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]amino]-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names Succinyl-ara-C

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:55726-37-9 SDS

55726-37-9Downstream Products

55726-37-9Relevant academic research and scientific papers

Synthesis and reactivity of 5-fluorouracil/cytarabine mutual prodrugs

Menger, Fredric M.,Rourk, Michael J.

, p. 9083 - 9088 (2007/10/03)

Two mutual prodrugs, in which two different anti-cancer drugs are attached to the same molecule via labile linkages, are synthesized and examined kinetically. One of the mutual prodrugs loses a drug component under physiological conditions within an hour, but the other mutual prodrug (having a longer spacer between the two drugs) is stable to chemical degradation even at hither pH values. Thus, enzymatic hydrolysis alone will release the two anti-cancer drugs. The potential value of anti-cancer mutual prodrugs is discussed.

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