3095-38-3 Usage
Description
3,5-Dimethyl-4-nitrobenzoic acid is an organic compound characterized by its molecular structure featuring a benzoic acid backbone with methyl groups at the 3rd and 5th positions and a nitro group at the 4th position. It is a versatile chemical intermediate with a wide range of applications across different industries due to its unique properties.
Uses
Used in Organic Synthesis:
3,5-Dimethyl-4-nitrobenzoic acid is used as a key intermediate for the synthesis of various organic compounds. Its presence in the molecular structure allows for further functionalization and modification, making it a valuable building block in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3,5-Dimethyl-4-nitrobenzoic acid is utilized as a starting material for the development of new drugs. Its unique structure can be modified to create active pharmaceutical ingredients (APIs) with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemicals:
3,5-Dimethyl-4-nitrobenzoic acid is employed as a crucial component in the formulation of agrochemicals, such as pesticides and herbicides. Its chemical properties enable it to be incorporated into these products to enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Dyestuff Industry:
In the dyestuff industry, 3,5-Dimethyl-4-nitrobenzoic acid is used as a raw material for the production of various dyes and pigments. Its chemical structure allows for the creation of a diverse range of colorants that can be used in different applications, such as textiles, plastics, and printing inks, to impart vibrant and long-lasting colors.
Check Digit Verification of cas no
The CAS Registry Mumber 3095-38-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,9 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3095-38:
(6*3)+(5*0)+(4*9)+(3*5)+(2*3)+(1*8)=83
83 % 10 = 3
So 3095-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c1-5-3-7(9(11)12)4-6(2)8(5)10(13)14/h3-4H,1-2H3,(H,11,12)
3095-38-3Relevant articles and documents
POLYCYCLIC AMINES AS OPIOID RECEPTOR MODULATORS
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Paragraph 0129; 0289, (2018/10/11)
The present invention provides a genus of polycyclic amines that are useful as opioid receptor modulators. The compounds of the invention are useful in both therapeutic and diagnostic methods, including for treating pain, neurological disorders, cardiac disorders, bowel disorders, drug and alcohol addiction, drug overdose, urinary disorders, respiratory disorders, sexual dysfunction, psoriasis, graft rejection or cancer.
Chemoselective reduction and self-immolation based FRET probes for detecting hydrogen sulfide in solution and in cells
Chen, Bifeng,Wang, Peng,Jin, Qingqing,Tang, Xinjing
supporting information, p. 5629 - 5633 (2014/07/22)
Hydrogen sulfide (H2S) has been regarded as the third gaseous transmitter. Based on the mechanism of chemoselective azido reduction and self-immolation, five fluorescence resonance energy transfer (FRET) probes for the detection of H2S were designed and synthesized. The effect of functional substitution of the self-immolative moiety on azido reduction and quinone-methide rearrangement were investigated. Their fluorescence responses and chemoselectivity for H2S detection were evaluated in solutions and in cells. This strategy may provide a general route for designing H 2S probes with many commercially available FRET pairs. the Partner Organisations 2014.
Peroxynitrite generation from a NO-releasing nitrobenzene derivative in response to photoirradiation
Ieda, Naoya,Nakagawa, Hidehiko,Horinouchi, Taeko,Peng, Tao,Yang, Dan,Tsumoto, Hiroki,Suzuki, Takayoshi,Fukuhara, Kiyoshi,Miyata, Naoki
supporting information; experimental part, p. 6449 - 6451 (2011/06/27)
Photocontrollable ONOO- generation from a nitrobenzene derivative was demonstrated. The designed compound released NO in response to photoirradiation, and the resulting semiquinone reduced molecular oxygen to generate O2-; reaction of the two generated ONOO -, as confirmed with an ONOO- fluorescent probe, HKGreen-3.