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tert-Butyl 3,5-dinitrobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5342-97-2

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5342-97-2 Usage

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 4415, 1994 DOI: 10.1016/S0040-4039(00)73371-5

Check Digit Verification of cas no

The CAS Registry Mumber 5342-97-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5342-97:
(6*5)+(5*3)+(4*4)+(3*2)+(2*9)+(1*7)=92
92 % 10 = 2
So 5342-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O6/c1-11(2,3)19-10(14)7-4-8(12(15)16)6-9(5-7)13(17)18/h4-6H,1-3H3

5342-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 3,5-dinitrobenzoate

1.2 Other means of identification

Product number -
Other names t-butyl 3,5-dinitrobenzoate

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:5342-97-2 SDS

5342-97-2Relevant academic research and scientific papers

Innovative Multipodal Ligands Derived from Tr?ger's Bases for the Sensitization of Lanthanide(III) Luminescence

Barja, Beatriz C.,Bruttomesso, Andrea C.,Eliseeva, Svetlana V.,Petoud, Stéphane,Ramírez, Javier A.,Trupp, Leandro,Vardé, Mariana

supporting information, p. 16900 - 16909 (2020/11/30)

Herein, the synthesis and characterization of the first family of multipodal ligands with a Tr?ger's base framework designed for the preparation of luminescent lanthanide(III) complexes are reported. Eight ligands were designed and synthesized using diffe

Supramolecular graft copolymers in moderately polar media based on hydrogen-bonded aromatic oligoamide units

Pan, Xusong,Chen, Chao,Peng, Jiang,Yang, Yongan,Wang, Yinghan,Feng, Wen,Deng, Pengchi,Yuan, Lihua

supporting information, p. 9510 - 9512 (2012/11/06)

By exploiting hetero-complementary aromatic oligoamide units containing hextuple hydrogen bonds, supramolecular graft copolymers were successfully constructed in moderately polar media.

A novel, general route to the synthesis of carboxylic acid esters and thiolesters

Sucheta,Reddy,Ravi,Rama Rao

, p. 4415 - 4416 (2007/10/02)

Carboxylic acids were conveniently esterified with alcohols and thiols by the use of triphenylphosphine and N-bromo/Iodo succinimide to afford the corresponding esters and thiol esters.

REAGENTS AND SYNTHETIC METHODS 28. MODIFIED PROCEDURES FOR ANHYDRIZATION, ESTERIFICATION AND THIOLESTERIFICATION OF CARBOXYLIC ACIDS BY MEANS OF AVAILABLE PHOSPHORUS REAGENTS.

Arrieta, A.,Garcia, T.,Lago, J. M.,Palomo, C.

, p. 471 - 488 (2007/10/02)

Carboxylic acid anhydrides, esters and thiol esters are obtained by a one-pot method from carboxylic acids and alcohols or thiol by means of phosphorus oxychloride or phenyl dichlorophosphoridate reagents.

Esterification of Aromatic Carboxylic Acids with Alcohols Using 2-Chloro-3,5-dinitropyridine as a Condensing Agent

Takimoto, Seiji,Abe, Naomi,Kodera, Yasushi,Ohta, Hiroshi

, p. 639 - 640 (2007/10/02)

The reaction of 2-chloro-3,5-dinitropyridine (CDNP) with carboxylic acids and alcohols was examined, and it was found that CDNP was a useful condensing agent.Various esters were prepared in good yields.

Esterification of Carboxylic Acids with Alcohols Using Benzenesulphonyl and Methanesulphonyl Chlorides

Dharmaratne, H. R. W.,Gunatilaka, A. A. Leslie,Sotheeswaran, S.

, p. 39 - 41 (2007/10/02)

The role of benzene- and methane-sulphonyl chlorides as coupling agents in the esterification of carboxylic acids with alcohols has been investigated.Hindered tertiary alcohols require initial conversion of the acid to the mixed acid-anhydride with benzenesulphonyl chloride.It is necessary to adjust molar ratios for esterification with secondary alcohols so that the intermediate formed is the symmetrical acid anhydride, since mixed acid-anhydrides also give the sulphonates of the alcohols wihich are difficult to separate from the esters.

Esterification of Carboxylic Acids by Alcohols with 2-Chloro-1,3,5-trinitrobenzene as Condensing Agent

Takimoto, Seiji,Inanaga, Junji,Katsuki, Tsutomu,Yamaguchi, Masaru

, p. 1470 - 1473 (2007/10/02)

When mixtures of carboxylic acids or their sodium salts and alcohols were treatment with 2-chloro-1,3,5-trinitrobenzene in the presence of pyridine under mild conditions, the corresponding carboxylic esters were formed.The yields and the rates of the ester formation depended on the types of the acids and the alcohols used.

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