2207-68-3 Usage
Description
1-(4-Nitrophenyl)glycerol is a white to light yellow crystalline powder that serves as a valuable compound in various applications due to its unique chemical properties.
Uses
Used in Bacterial Control:
1-(4-Nitrophenyl)glycerol is used as an additive for controlling the swarming of Proteus bacteria on culture media. It helps in managing the growth and spread of these bacteria, which can be particularly useful in laboratory settings and medical research.
Used in Inhibiting Bacterial Behavior and Virulence:
1-(4-Nitrophenyl)glycerol is used as an inhibitor to regulate the swarming behavior and virulence factor expression in Proteus mirabilis. By inhibiting these activities, it can potentially reduce the pathogenicity of the bacteria, making it a valuable tool in the study and control of bacterial infections.
Used in Pharmaceutical Industry:
1-(4-Nitrophenyl)glycerol can be used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a key component in the development of new drugs and therapies.
Used in Chemical Research:
1-(4-Nitrophenyl)glycerol is used as a research compound in the field of chemistry. Its properties make it an interesting subject for studying various chemical reactions and mechanisms, contributing to the advancement of scientific knowledge in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 2207-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2207-68:
(6*2)+(5*2)+(4*0)+(3*7)+(2*6)+(1*8)=63
63 % 10 = 3
So 2207-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO5/c11-5-8(12)6-15-9-3-1-7(2-4-9)10(13)14/h1-4,8,11-12H,5-6H2
2207-68-3Relevant articles and documents
Tandem Benzylic Oxidation/Dihydroxylation of α-Vinyl- and α-Alkenylbenzyl Alcohols
Fernandes, Rodney A.,Kattanguru, Pullaiah
, p. 92 - 107 (2015/10/19)
A de novo tandem benzylic oxidative dihydroxylation of α-vinyl- and α-alkenylbenzyl alcohols has been developed to give α,β-dihydroxypropiophenones (=2,3-dihydroxy-1-phenylpropan-1-ones) and α,β-dihydroxyalkyl phenones. This method was shown to be substrate-selective and specific for the oxidation of benzylic alcohols.
