13300-60-2 Usage
Derivative of benzoic acid
2,5-Dichloro-4-nitrobenzoic acid is derived from benzoic acid, which means it is a modified version of the parent compound with additional functional groups.
Presence of two chlorine atoms and one nitro group
The presence of these atoms on the benzene ring contributes to the compound's chemical properties and reactivity.
Commonly used in synthesis
2,5-Dichloro-4-nitrobenzoic acid is used in the synthesis of various pharmaceuticals, agrochemicals, and dyes, making it an important intermediate compound in the production of these products.
Yellow crystalline solid
The physical appearance of 2,5-Dichloro-4-nitrobenzoic acid is a yellow crystalline solid, which can be useful for identification and handling purposes.
Sparingly soluble in water
This property means that the compound does not dissolve easily in water, which can affect its solubility and reactivity in aqueous solutions.
Soluble in organic solvents
2,5-Dichloro-4-nitrobenzoic acid dissolves more readily in organic solvents, which can be important for its use in chemical reactions and processes.
Safety precautions
It is important to handle 2,5-Dichloro-4-nitrobenzoic acid with care and follow proper safety protocols when working with it in a laboratory setting, as it may pose potential hazards or risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 13300-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13300-60:
(7*1)+(6*3)+(5*3)+(4*0)+(3*0)+(2*6)+(1*0)=52
52 % 10 = 2
So 13300-60-2 is a valid CAS Registry Number.
13300-60-2Relevant articles and documents
Process for the preparation of fluorinated benzoic acids
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, (2008/06/13)
A process for the preparation of 2-chloro-4,5-difluorobenzoic acid and 2,4,5-trifluorobenzoic acid as well as synthetic intermediates useful in and prepared according thereto, comprising reacting a nitrobenzene having the formula STR1 wherein X is chloro or fluoro, with an appropriate carbanion to form a compound having the formula STR2 wherein one of Y and Z is chloro and the other is nitro, and R is a radical selected from the group consisting of --CCl3, --CH2 NO2, --CH(NO2)R1, --CH(CO2 R1)2, --CH(C(O)R2)2, --CH(CN)CO2 R1, --CH(CO2 R1)COR2 and --COR2 where R1 is alkyl or arylalkyl and R2 is alkyl, aryl or arylalkyl and, where appearing more than once in such a radical, R1 and R2 may be the same or different at each occurrence.
