5485-88-1 Usage
Uses
Used in Pharmaceutical Industry:
3-CHLORO-4-HYDROXY-5-METHOXYBENZONITRILE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical industry, 3-CHLORO-4-HYDROXY-5-METHOXYBENZONITRILE is utilized as a precursor in the production of agrochemicals, which can help in the development of pesticides and other agricultural products to improve crop yields and protect plants from diseases.
Used for Antimicrobial Applications:
3-CHLORO-4-HYDROXY-5-METHOXYBENZONITRILE is employed for its antimicrobial properties, which can be useful in various applications such as disinfectants, sanitizers, and preservatives to control the growth of harmful microorganisms.
Used for Antioxidant Applications:
The antioxidant properties of 3-CHLORO-4-HYDROXY-5-METHOXYBENZONITRILE make it a potential candidate for use in applications requiring protection against oxidative stress, such as in the food industry to extend the shelf life of products or in cosmetic formulations to protect against environmental damage.
Check Digit Verification of cas no
The CAS Registry Mumber 5485-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,8 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5485-88:
(6*5)+(5*4)+(4*8)+(3*5)+(2*8)+(1*8)=121
121 % 10 = 1
So 5485-88-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClNO2/c1-12-7-3-5(4-10)2-6(9)8(7)11/h2-3,11H,1H3
5485-88-1Relevant academic research and scientific papers
Ruthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: A new route to halogenated aromatic nitriles
Chinnagolla, Ravi Kiran,Pimparkar, Sandeep,Jeganmohan, Masilamani
supporting information, p. 3146 - 3148 (2013/06/04)
The intramolecular halogenation of O-methylbenzohydroximoyl halides in the presence of a Ru catalyst and the ligand diphenylacetylene afforded halo substituted aromatic nitriles in a highly regioselective manner. Further, substituted nitriles were converted into substituted tetrazole derivatives in the presence of NaN3 and I2.
NOVEL AMINOMETHYL BENZENE DERIVATIVES
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Page/Page column 30, (2009/10/22)
The invention relates to novel aminomethyl benzene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunomodulating agents. (I) wherein A represents one of the groups (I), (I), (I) and
Synthesis and Antitubercular Activity of 4-(5-Nitro-2-furyl/2-pyrazinyl/1-adamantyl)-2-(alkyl/aryl/arylamino)thiazoles
Khadse, B. G.,Lokhande, S. R.,Bhamaria, R. P.,Prabhu, S. R.
, p. 856 - 860 (2007/10/02)
The reaction of haloketones, obtained from Arndt-Eistert reaction on the acid chlorides of 1-adamantane, 5-nitrofuroic acid and pyrazine-2-carboxylic acid, with different thioamides and thioureas affords the title thiazoles (I-III).Some of them exhibit interesting antitubercular activity at 6.25 to 0.38 μg/ml concentration against H37Rv strain of M. tubercolosis in vitro testing.The structure activity relationship (SAR) has also been discussed.
