101870-78-4 Usage
General Description
6-Isopropylpyridin-3-ol, also known as 3-(1-methylethyl)pyridin-6-ol, is a chemical compound with the molecular formula C8H11NO. It is a white solid with a molecular weight of 137.179 g/mol. 6-Isopropylpyridin-3-ol is classified as a pyridine derivative and is commonly used in the production of various pharmaceuticals and agrochemicals. It is known for its antimicrobial properties and is used as an ingredient in some cosmetic and personal care products. Additionally, 6-Isopropylpyridin-3-ol has potential applications in the development of insecticides and other pest control products due to its insecticidal properties. It is important to handle this chemical with care and follow proper safety precautions, as it can be harmful if inhaled or ingested.
Check Digit Verification of cas no
The CAS Registry Mumber 101870-78-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,8,7 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101870-78:
(8*1)+(7*0)+(6*1)+(5*8)+(4*7)+(3*0)+(2*7)+(1*8)=104
104 % 10 = 4
So 101870-78-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-6(2)8-4-3-7(10)5-9-8/h3-6,10H,1-2H3
101870-78-4Relevant articles and documents
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives
Westaway, Susan M.,Preston, Alex G. S.,Barker, Michael D.,Brown, Fiona,Brown, Jack A.,Campbell, Matthew,Chung, Chun-Wa,Drewes, Gerard,Eagle, Robert,Garton, Neil,Gordon, Laurie,Haslam, Carl,Hayhow, Thomas G.,Humphreys, Philip G.,Joberty, Gerard,Katso, Roy,Kruidenier, Laurens,Leveridge, Melanie,Pemberton, Michelle,Rioja, Inma,Seal, Gail A.,Shipley, Tracy,Singh, Onkar,Suckling, Colin J.,Taylor, Joanna,Thomas, Pamela,Wilson, David M.,Lee, Kevin,Prinjha, Rab K.
, p. 1370 - 1387 (2016/03/05)
Following the discovery of cell penetrant pyridine-4-carboxylate inhibitors of the KDM4 (JMJD2) and KDM5 (JARID1) families of histone lysine demethylases (e.g., 1), further optimization led to the identification of non-carboxylate inhibitors derived from pyrido[3,4-d]pyrimidin-4(3H)-one. A number of exemplars such as compound 41 possess interesting activity profiles in KDM4C and KDM5C biochemical and target-specific, cellular mechanistic assays.
