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Benzoic acid, 3,5-dinitro-, 1-methylpropyl ester is a chemical compound with the molecular formula C10H11NO5. It is an ester derivative of benzoic acid, where the hydroxyl group (-OH) is replaced by an ester group derived from 1-methylpropyl (also known as isobutyl) alcohol. The compound features a benzene ring with two nitro groups (-NO2) at the 3rd and 5th positions, which imparts a strong, pungent odor. This chemical is primarily used as a plasticizer, a substance added to plastics to increase their flexibility and workability. It is also used in the production of certain types of resins and as a chemical intermediate in the synthesis of other organic compounds. Due to its potential health and environmental risks, handling and disposal of Benzoic acid, 3,5-dinitro-, 1-Methylpropyl ester must be done with proper safety measures and in accordance with local regulations.

7510-57-8

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7510-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7510-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7510-57:
(6*7)+(5*5)+(4*1)+(3*0)+(2*5)+(1*7)=88
88 % 10 = 8
So 7510-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O6/c1-3-7(2)19-11(14)8-4-9(12(15)16)6-10(5-8)13(17)18/h4-7H,3H2,1-2H3

7510-57-8Downstream Products

7510-57-8Relevant academic research and scientific papers

Nitrosation of the N-Alkyl-O-acylhydroxylamines. A New Deamination Method.

White, Emil H.,Ribi, Max,Cho, Lee K.,Egger, Notker,Dzadzic, Petar M.,Todd, Michael J.

, p. 4866 - 4871 (2007/10/02)

The nitrosation of N-alkyl-O-acylhydroxylamines leads to immediate decomposition at dry ice temperatures; the corresponding ester and nitrous oxide are formed.An 18O study has shown that the nitroso-O-acylhydroxylamines fragment directly rather than undergo a rearrangement reaction (as observed with the nitrosoamides).The product yields are respectable, especially at low tempreatures, and the method has promise for the generation of high energy carbonium ions.

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