1160-35-6 Usage
Uses
Used in Pharmaceutical Industry:
3-Pyridinecarbamonitrile,4-hydroxy-(6CI) is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activity and ability to be incorporated into complex molecular structures.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Pyridinecarbamonitrile,4-hydroxy-(6CI) is used as a building block in the development of agrochemicals, contributing to the creation of compounds with specific pesticidal or herbicidal properties.
Used in Organic Synthesis:
3-Pyridinecarbamonitrile,4-hydroxy-(6CI) is utilized as a key component in organic synthesis, allowing for the formation of a wide range of organic compounds with diverse applications in various industries.
Used in Drug Discovery and Development:
Due to its biological activity, 3-Pyridinecarbamonitrile,4-hydroxy-(6CI) is employed as a potential candidate in drug discovery and development, where it may contribute to the creation of new therapeutic agents with novel mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 1160-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1160-35:
(6*1)+(5*1)+(4*6)+(3*0)+(2*3)+(1*5)=46
46 % 10 = 6
So 1160-35-6 is a valid CAS Registry Number.
1160-35-6Relevant academic research and scientific papers
Kubo, Isao,Fujita, Ken-ichi,Nihei, Ken-ichi,Masuoka, Noriyoshi
, p. 573 - 580 (2003)
Dodecyl (C12) gallate (3,4,5-trihydroxybenzoate) (1) was found to possess antibacterial activity specifically against Gram-positive bacteria, in addition to its potent antioxidant activity. The time-kill curve study indicates that this amphipathic gallate exhibits bactericidal activity against methicillin resistant Staphylococcus aureus (MRSA) strains. Dodecyl (lauryl) gallate inhibited oxygen consumption in whole cells and oxidation of NADH in membrane preparation. The antibacterial activity of this gallate comes in part from its ability to inhibit the membrane respiratory chain. As far as alkyl gallates are concerned, their antimicrobial spectra and potency depend in part on the hydrophobic portion of the molecule.
