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Vinleucinol, also known as 3-(4-vinylphenyl)-2-oxazolidinone, is a synthetic organic compound that has gained attention for its potential use in various applications, including as a monomer in polymer chemistry and as a building block for the synthesis of more complex molecules. It features a vinyl group attached to a phenyl ring, which allows for further chemical reactions and cross-linking, and a 2-oxazolidinone ring, which contributes to its stability and reactivity. Vinleucinol's unique structure makes it a promising candidate for the development of new materials with specific properties, such as improved mechanical strength or chemical resistance.

81571-28-0

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81571-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81571-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,7 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81571-28:
(7*8)+(6*1)+(5*5)+(4*7)+(3*1)+(2*2)+(1*8)=130
130 % 10 = 0
So 81571-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C51H69N5O8/c1-9-31(5)40(42(57)64-12-4)53-45(58)51(61)29-47(10-2)19-15-21-56-23-20-49(43(47)56)35-24-36(39(62-7)25-38(35)54(6)44(49)51)50(46(59)63-8)27-32-26-48(60,11-3)30-55(28-32)22-18-34-33-16-13-14-17-37(33)52-41(34)50/h13-17,19,24-25,31-32,40,43-44,52,60-61H,9-12,18,20-23,26-30H2,1-8H3,(H,53,58)/t31-,32+,40-,43-,44+,47-,48-,49+,50-,51+/m0/s1

81571-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Vinleucinol

1.2 Other means of identification

Product number -
Other names VILE

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:81571-28-0 SDS

81571-28-0Downstream Products

81571-28-0Relevant academic research and scientific papers

Vinblastin-23-oyl Amino Acid Derivatives: Chemistry, Physicochemical Data, Toxicity, and Antitumor Activities against P388 and L1210 Leukemias

Rao, Kandukuri S. P. Bhushana,Collard, Marie-Paule M.,Dejonghe, Jean Paul C.,Atassi, Ghanen,Hannart, Jean A.,Trouet, Andre

, p. 1079 - 1088 (2007/10/02)

The dimeric alkaloids vinblastine (VLB) and vincristine (VCR) differ structurally only in the functional group on the dihydroindole nitrogen.The semisynthetic derivative vindesine (VDS) differs slightly from VLB by having an amide group instead of an ester group.However, these minor distinctions are responsible for profound differences in the oncolytic spectrum, potency, and toxicity of these compounds.Vinblastin-23-oyl amino acid derivatives were synthesized by linking amino acid carboxylic esters to the vinblastin-23-oyl moiety through an amide linkage.Studies were extended to explore the influence of the nature of the amino acid, the ester alkyl chain lenghts, the stereoisomerism of the amino acid, or the reacetylation of the hydroxyl group (position O-4) of the vindoline moiety.The present study deals with the synthesis of 21 vinblastin-23-oyl amino acid derivatives, some of their physicochemical data, the acute toxicity in mice, and therapeutic activities of these derivatives against the P388 and L1210 leukemias in comparison with VDS, VBL, and VCR.

ON THE AMIDATION OT 17-DEACETYL-VINBLASTINE WITH THE ETHYLESTERS OF SOME AMINOACIDS

Rao, Bhushana K. S. P.,Collard, M. P.,Trouet, A.,Bruyn, A. De,Verzele, M.,et. al

, p. 133 - 140 (2007/10/02)

We described the synthesis of amides between 17-deacetylvinblastine (1) and the ethyl esters of valine (2), leucine (3), isoleucine (4), tryptophane (5) and valine-tryptophane (6).

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