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N-(2,4-Dinitrophenyl)proline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10200-25-6

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10200-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10200-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,0 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10200-25:
(7*1)+(6*0)+(5*2)+(4*0)+(3*0)+(2*2)+(1*5)=26
26 % 10 = 6
So 10200-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3O6/c15-11(16)9-2-1-5-12(9)8-4-3-7(13(17)18)6-10(8)14(19)20/h3-4,6,9H,1-2,5H2,(H,15,16)

10200-25-6SDS

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 1-(2,4-Dinitrophenyl)proline

1.2 Other means of identification

Product number -
Other names N-(2,4-dinitrophenyl)piperidine-2-carboxylic acid

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:10200-25-6 SDS

10200-25-6Relevant academic research and scientific papers

Synthesis of tri- and tetracyclic condensed quinoxalin-2-ones fused across the C-3 - N-4 bond

Chicharro, Roberto,De Castro, Sonia,Reino, Jose L.,Aran, Vicente J.

, p. 2314 - 2326 (2007/10/03)

We have studied the preparation of some fused quinoxalinones by Stevens rearrangement of a spiro-quinoxaline-derived ammonium ylide or by treatment of N-(2,4-dinitrophenyl)-and N-(2-nitrophenyl)imino acids with different reducing agents. We have reinvestigated and clarified some related processes found in the literature starting from imino acids derivatives. Additional reactions of the fused quinoxalinones, as well as the useful dehydrogenation/decarboxylation of some easily available 1-arylindoline-2-carboxylic acids to the corresponding 1-arylindoles, are also reported. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

1,2,4-TRINITROBENZENE AS A THIOL REAGENT

Takahashi, Seitaro,Kokubo, Masayuki,Satake, Kazuo

, p. 1445 - 1448 (2007/10/02)

The 2,4-dinitrophenylation of thiol or amino group with 1,2,4-trinitrobenzene proceeded quantitatively at pH 8.5 and 30 deg C.The rate of S-dinitrophenylation was ca. 1E4 times faster than that of N-dinitrophenylation.So this reaction can be used for both the determination of thiol even in the presence of large excess amine and the specific modification of thiol in proteins.

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