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21161-11-5

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21161-11-5 Usage

Uses

2-Nitroisophthalic Acid is an intermediate in the synthesis of 2,6-Dihydroxymethyl Rilpivirine (D446615), which is an analog of Rilpivirine (R509800) a novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent.

Check Digit Verification of cas no

The CAS Registry Mumber 21161-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,6 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21161-11:
(7*2)+(6*1)+(5*1)+(4*6)+(3*1)+(2*1)+(1*1)=55
55 % 10 = 5
So 21161-11-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5NO6/c10-7(11)4-2-1-3-5(8(12)13)6(4)9(14)15/h1-3H,(H,10,11)(H,12,13)

21161-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Nitroisophthalic acid

1.2 Other means of identification

Product number -
Other names 2-nitrobenzene-1,3-dicarboxylic 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:21161-11-5 SDS

21161-11-5Relevant articles and documents

3,3′-Diiodobinaphthol and 3,3′-Diiodobiphenol Derivatives as Hypervalent Iodine Organocatalysts for the α-Oxytosylation of Ketones

Brenet, Simon,Minozzi, Clémentine,Clarens, Bastien,Amiri, Lilia,Berthiol, Florian

, p. 3859 - 3873 (2015)

New series of enantiopure 3,3′-diiodobinaphthol- and 3,3′-diiodobiphenol-based molecules have been synthesized and used as chiral hypervalent iodine oxidation organocatalysts in the α-oxytosylation of propiophenone. When we compared these new organocatalysts to our previous series of 3,3′-diiodo-1,1′-binaphthalene-2,2′-diol-fused maleimides, we have made two important observations: the maleimide moiety is the best moiety for obtaining moderate enantioselectivities, and the presence of an aliphatic substituent on the biaryl part of the catalyst enhances the enantioselectivity.

SELF-IMMOLATIVE SYSTEMS

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Page/Page column 11; 26; 27, (2020/05/28)

The present invention is concerned with self-immolative recognition and/or responsive systems for electrophilic compounds, especially alkylating agents, which systems may comprise disclosure or detection of the alkylating agent. The present invention is especially concerned with non-protic triggered self-immolative systems, molecules, and methods, and in particular for detection of non- protic electrophilic agents, and especially alkylating agents, for example alkyl or benzylic halides, which may be found in pesticides or fumigants, or chemical warfare agents.

PROGRAMMED DEGRADATION OF POLYMERS DERIVED FROM BIOMASS

-

, (2016/05/10)

Novel photodegradable polymers derived from biomass are provided, together with methods of making and methods of using said polymers.

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