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NSC210729, also known as 2-(4-morpholinyl)-5-nitrobenzothiazole, is a synthetic chemical compound with the molecular formula C11H10N4O3S. It is a yellow crystalline solid with a molecular weight of 286.29 g/mol. NSC210729 has been studied for its potential antitumor and anti-inflammatory properties, as well as its ability to inhibit certain enzymes involved in cell signaling pathways. The compound is part of the National Cancer Institute's (NCI) database of small molecules, which are screened for potential therapeutic applications. Its chemical structure features a benzothiazole core with a nitro group at the 5-position and a morpholine group at the 2-position, which contributes to its biological activity.

5615-90-7

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5615-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5615-90-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5615-90:
(6*5)+(5*6)+(4*1)+(3*5)+(2*9)+(1*0)=97
97 % 10 = 7
So 5615-90-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H20N2O3/c1-2-5-11-12(18-19)10-13(14-6-3-8-20-14)17-16(11)15-7-4-9-21-15/h3-4,6-9,11,13,16-17,19H,2,5,10H2,1H3/b18-12-

5615-90-7SDS

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 3-methylpyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names (+/-)-3-Methylsuccinimide

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:5615-90-7 SDS

5615-90-7Relevant academic research and scientific papers

Carbonylation (hydroformylation and hydrocarbalkoxylation) and enantioselective carbonylation of some methacrylic acid derivatives

Consiglio, Giambattista,Kollar, Laszlo,Koelliker, Robert

, p. 375 - 383 (2007/10/02)

The hydroformylation of methyl methacrylate (1) or t-butyl methacrylate (2) takes place with fair to good chemoselectivity, the regioselectivity depending on the catalyst precursor used.By contrast, methacrylonitrile (3), methacrylamide (4), and N-benzyl-methacrylamide (5) undergo hydroformylation followed by subsequent reactions.The formyl product formed is reduced to the corresponding 2-cyano-2-methylpropan-1-ol in the case of 3, and undergoes cyclization to 2-methyl-2,3-dehydrobutyrolactames for 4 and 5.Under conditions of hydrocarbalkoxylation in the presence of palladium catalysts, 4 gives 3-methylsuccinimide.In the enantioselective reactions, extents of asymmetric induction of about 20-50percent have been obtained.

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