7151-68-0 Usage
Description
3-Methoxy-4-methylbenzoic acid is an organic compound characterized by the presence of a methoxy group at the 3rd position and a methyl group at the 4th position on a benzene ring. It possesses a carboxylic acid functional group, which gives it acidic properties. 3-Methoxy-4-methylbenzoic acid is known for its potential applications in various fields, particularly in the synthesis of bioactive molecules.
Uses
Used in Pharmaceutical Industry:
3-Methoxy-4-methylbenzoic acid is used as a key intermediate in the synthesis of acyl pentapetide lactone, a component of actinomycin, which is produced by certain Streptomyces bacteria. Actinomycin and its derivatives have been recognized for their potent antibiotic and antitumor properties, making this compound an essential building block in the development of new therapeutic agents.
Additionally, due to its unique structural features, 3-Methoxy-4-methylbenzoic acid may also be utilized in the design and synthesis of other bioactive compounds, such as pharmaceuticals, agrochemicals, and materials with specific properties. Its versatility in chemical reactions and potential to be modified or functionalized further expands its applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 7151-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7151-68:
(6*7)+(5*1)+(4*5)+(3*1)+(2*6)+(1*8)=90
90 % 10 = 0
So 7151-68-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c1-6-3-4-7(9(10)11)5-8(6)12-2/h3-5H,1-2H3,(H,10,11)/p-1
7151-68-0Relevant articles and documents
Toward a better understanding on the mechanism of ortholithiation. Tuning of selectivities in the metalation of meta-anisic acid by an appropriate choice of base
Nguyen, Thi-Huu,Chau, Nguyet Trang Thanh,Castanet, Anne-Sophie,Nguyen, Kim Phi Phung,Mortier, Jacques
, p. 2445 - 2448 (2007/10/03)
(Chemical Equation Presented) If employed in THF at 0°C, LTMP metalates meta-anisic acid at the doubly activated position. In contrast, n-BuLi/t-BuOK deprotonates position C-4 preferentially at low temperature. Functionalization at C-6 requires protection of the C-2 site beforehand. As a result of these findings, a new mechanism is proposed for the heteroatom-directed ortholithiation of aromatic compounds.
Baker's yeast-mediated enantioselective synthesis of the bisabolane sesquiterpenes (+)-curcuphenol, (+)-xanthorrhizol, (-)-curcuquinone and (+)-curcuhydroquinone
Fuganti, Claudio,Serra, Stefano
, p. 3758 - 3764 (2007/10/03)
Fermenting baker's yeast converts the unsaturated aldehydes 5a-c into the saturated alcohols 6a-c, respectively. The microbial saturation of substrates adsorbed on a nonpolar resin proceeds in high chemical yields and shows complete enantioselectivity in the formation of the (S)-(+) isomers. Enantiopure 6a-c are versatile chiral building blocks for the synthesis of bisabolane sesquiterpenes. Their usefulness is shown in the preparation of (S)-(+)-curcuphenol, (S)-(+)-xanthorrhizol, (S)-(-)-curcuquinone and (S)-(+)-curcuhydroquinone. The Royal Society of Chemistry 2000.