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(S)-(-)-2-OXO-1,5-IMIDAZOLIDINEDICARBOXYLIC ACID 1-BENZYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59760-01-9

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59760-01-9 Usage

Uses

Z-protected imidazolidinone for sequential N-alkylation.

Check Digit Verification of cas no

The CAS Registry Mumber 59760-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,6 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59760-01:
(7*5)+(6*9)+(5*7)+(4*6)+(3*0)+(2*0)+(1*1)=149
149 % 10 = 9
So 59760-01-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O5/c15-10(16)9-6-13-11(17)14(9)12(18)19-7-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,13,17)(H,15,16)/t9-/m0/s1

59760-01-9 Well-known Company Product Price

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  • Aldrich

  • (392308)  (S)-(−)-1-Z-2-Oxo-5-imidazolidinecarboxylicacid  98%

  • 59760-01-9

  • 392308-1G

  • 508.95CNY

  • Detail
  • Aldrich

  • (392308)  (S)-(−)-1-Z-2-Oxo-5-imidazolidinecarboxylicacid  98%

  • 59760-01-9

  • 392308-5G

  • 1,964.43CNY

  • Detail

59760-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-2-oxo-3-phenylmethoxycarbonylimidazolidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names (S)-2-oxo-imidazolidine-1,5-dicarboxylic acid-1-benzyl ester

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:59760-01-9 SDS

59760-01-9Relevant articles and documents

HETEROCYCLIC COMPOUNDS FOR USE IN THE TREATMENT OF CANCER

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Page/Page column 177, (2021/02/19)

The application relates to heterocyclic amide derivatives and their use in the treatment and prophylaxis of cancer, and to compositions containing said derivatives and processes for their preparation. (Formula (I))

Pyridine ketone compound and its composition and use thereof (by machine translation)

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Paragraph 0261; 0263; 0264, (2017/08/25)

The invention relates to the field of blood coagulation. In particular, the invention relates to a pyridone compound, or a stereoisomer thereof, tautomers, nitrogen oxide, solvate, metabolite, pharmaceutically acceptable salt or prodrug and pharmaceutical composition containing the compound. The invention also relates to such compounds and pharmaceutical composition preparation method, and they in preparing for the prevention, treatment or alleviation of patient Xa factor relative thromboembolic disease in use. (by machine translation)

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

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Page/Page column, (2015/02/19)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

THERAPEUTICALLY ACTIVE COMPOUNDS AND USE THEREOF

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Page/Page column 162, (2015/02/19)

Provided are therapeutically active compounds and the use in manufacture of medicaments for treating a cancer characterized by the presence of a mutant allele of IDH1.

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

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Page/Page column 163, (2015/02/19)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

THERAPEUTICALLY ACTIVE COMPOSITIONS AND THEIR METHODS OF USE

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Page/Page column, (2013/07/31)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

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Page/Page column 163, (2013/07/31)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

Identification of 2-oxo-N-(phenylmethyl)-4-imidazolidinecarboxamide antagonists of the P2X7 receptor

Abberley, Lee,Bebius, Aude,Beswick, Paul J.,Billinton, Andy,Collis, Katharine L.,Dean, David K.,Fonfria, Elena,Gleave, Robert J.,Medhurst, Stephen J.,Michel, Anton D.,Moses, Andrew P.,Patel, Sadhana,Roman, Shilina A.,Scoccitti, Tiziana,Smith, Beverley,Steadman, Jon G.A.,Walter, Daryl S.

scheme or table, p. 6370 - 6374 (2010/12/18)

A backup molecule to compound 2 was sought by targeting the most likely metabolically vulnerable site in this molecule. Compound 18 was subsequently identified as a potent P2X7 antagonist with very low in vivo clearance and high oral bioavailability in all species examined. Some evidence to support the role of P2X7 in the etiology of pain is also presented.

Synthesis of dirhodium(II) tetrakis[methyl 1-(3-phenylpropanoyl)-2- oxaimidazolidine-4(S)-carboxylate], Rh2(4S-MPPIM)4

Doyle, Michael P.,Colyer, John T.

, p. 3601 - 3604 (2007/10/03)

The large-scale synthesis with greatly improved yields of methyl 1-(3-phenylpropanoyl)-2-oxaimidazolidine-4(S)-carboxylate and the chiral dirhodium(II) carboxamidate derived from it, Rh2(4S-MPPIM) 4, is described. The key step in the

First attempts at differential diastereoselection in catalytic reactions of N-chirally substituted dirhodium(II) tetrakis[methyl 2-oxoimidazolidine-4(S)-carboxylates] with diazoacetates

Doyle,Timmons,Arndt,Duursma,Colyer,Bruenner

, p. 2156 - 2161 (2007/10/03)

Chiral attachments on 2-oxoimidazolidine-4(S)-carboxylate ligands for dirhodium(II) can provide differential diastereoselection in catalytic reactions of diazo compounds. The synthesis of these heterocyclic ligands from the readily available amino acid as

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