169310-05-8 Usage
General Description
3-Chloro-2-formylbenzoic acid is a chemical compound with the formula C8H5ClO3. It is a derivative of benzoic acid, with a chlorine atom and a formyl group attached to the benzene ring. 3-Choro-2-formylbenzoic acid is widely used in the synthesis of pharmaceuticals and agrochemicals due to its versatile reactivity and functional groups. It is also utilized in the production of dyes and pigments. In addition, 3-Chloro-2-formylbenzoic acid has applications in the field of materials science, such as in the development of liquid crystals and organic electronic devices. This chemical is considered to be a valuable building block in organic synthesis, and its properties make it an important ingredient in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 169310-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,3,1 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169310-05:
(8*1)+(7*6)+(6*9)+(5*3)+(4*1)+(3*0)+(2*0)+(1*5)=128
128 % 10 = 8
So 169310-05-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClO3/c9-7-3-1-2-5(8(11)12)6(7)4-10/h1-4H,(H,11,12)
169310-05-8Relevant articles and documents
CARBAZOLE COMPOUNDS AND METHODS OF USING SAME
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Paragraph 00109, (2015/02/25)
The present invention provides carbazole compounds of the formula (I), which can be used for treating microbial, protozoan, viral infections and cancer. ?
FUSED INDOLE COMPOUNDS AND METHODS OF USING SAME
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Page/Page column 00106; 00107, (2015/04/22)
The invention relates to fused indole compounds of formula (I) that can be used for treating microbial infections, in particular, fungal infections, and selectively kill cancer cells.
Ortho-metalation of unprotected 3-bromo and 3-chlorobenzoic acids with hindered lithium dialkylamides
Gohier, Frederic,Mortier, Jacques
, p. 2030 - 2033 (2007/10/03)
Upon treatment of 3-chloro/bromobenzoic acids with hindered lithium dialkylamides (LDA or LTMP) at -50 °C, lithium 3-chloro/bromo-2-lithiobenzoates are generated. These dianions can be trapped as such to afford after electrophilic quenching a variety of s
