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1,2-Benzisoxazole-3-carboxylic acid, 6-nitrois a chemical compound with the molecular formula C9H5NO6. It is a derivative of benzisoxazole, a heterocyclic compound. This chemical has a nitro group attached to the 6th position of the benzisoxazole ring. Its structure and properties make it useful for various applications in the field of medicinal and agricultural chemistry.
Used in Pharmaceutical Industry:
1,2-Benzisoxazole-3-carboxylic acid, 6-nitrois used as a building block for the preparation of pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
1,2-Benzisoxazole-3-carboxylic acid, 6-nitrois used as a building block for the preparation of agrochemicals. Its chemical properties and reactivity make it a useful component in the synthesis of pesticides and other agricultural chemicals.
Used in Organic Synthesis:
1,2-Benzisoxazole-3-carboxylic acid, 6-nitrois used in organic synthesis for the preparation of various organic compounds. Its reactivity and functional groups make it a versatile intermediate in the synthesis of a wide range of organic molecules.

28691-50-1

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28691-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28691-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,9 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28691-50:
(7*2)+(6*8)+(5*6)+(4*9)+(3*1)+(2*5)+(1*0)=141
141 % 10 = 1
So 28691-50-1 is a valid CAS Registry Number.

28691-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-1,2-benzoxazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-nitro-1,2-benzoxazole-3-carboxylato

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:28691-50-1 SDS

28691-50-1Relevant academic research and scientific papers

An indirect chaotropic mechanism for the stabilization of helix conformation of peptides in aqueous trifluoroethanol and hexafluoro-2- propanol

Walgers, Richard,Lee, Tony C.,Cammers-Goodwin, Arthur

, p. 5073 - 5079 (1998)

A revised indirect mechanism is proposed for the effect of 2,2,2- trifluoroethanol on peptide conformation (TFE effect) that suggest tighter solvent shells in pure water for helical states than random coil states. The alcoholic cosolvent stabilizes the he

Supramolecular kinetic effects by pillararenes: The synergism between spatiotemporal and preorganization concepts in decarboxylation reactions

Vieira Silveira, Eduardo,Montecinos, Rodrigo,Scorsin, Leandro,Garcia-Rio, Luis,Medeiros, Michelle,Nascimento, Vanessa,Nome, Faruk,Affeldt, Ricardo F.,Micke, Gustavo A.

, p. 6486 - 6494 (2021)

A study about spontaneous decarboxylation reactions of 3-carboxy-1,2-benzisoxazole (CBI) nitrated derivatives (6-NitroCBI and 5,6-DinitroCBI) compared with supramolecular kinetic effects promoted by two cationic pillararenes (P5A and P6A) has been carried

Applicaton of Stepwise Self-Association Models for the Analysis of Reaciton Rates in Aggregates of Tri-n-octylalkylammonium Salts

Biresaw, Girma,Bunton, Clifford A.

, p. 5854 - 5858 (2007/10/02)

Tri-n-octylalkylammonium salts, 1, form small, polydisperse aggregates and do not have a critical micelle concentration.Rate enhancements of decarboxylation of 6-nitrobenzisoxazolecarboxylate ion in 1c (alkyl = Et) and 1e (alkyl = 2-hydroxyethyl) and dephosphorylation of 2,4-dinitrophenyl phosphate were analyzed by using a one-parameter self-association scheme of aggregation.Reacitons of 2,4-dinitrochlorobenzene, bis(2,4-dinitrophenyl) phosphate and p-nitrophenyl diphenyl phosphate with 1e at high pH were analyzed by using a similar model.Better fits of the data were obtained than with schemes based on a simple mass-action model.

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