6641-05-0 Usage
Uses
Used in Pharmaceutical Industry:
(5-chloro-2-methoxybenzene-1,3-diyl)dimethanol is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique structural features allow it to be a valuable building block in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, (5-chloro-2-methoxybenzene-1,3-diyl)dimethanol is used as a starting material for the production of various agrochemicals. Its chemical properties make it suitable for the synthesis of compounds with pesticidal, herbicidal, or fungicidal activities.
Used in Polymer Industry:
(5-chloro-2-methoxybenzene-1,3-diyl)dimethanol is used as a monomer or a building block in the polymer industry. Its incorporation into polymer structures can lead to materials with enhanced properties, such as improved mechanical strength, thermal stability, or chemical resistance.
Used in Materials Science:
In the field of materials science, (5-chloro-2-methoxybenzene-1,3-diyl)dimethanol can be used to develop novel materials with specific properties. Its structural features may contribute to the creation of materials with unique optical, electronic, or magnetic characteristics.
Used in Specialty Chemicals Production:
(5-chloro-2-methoxybenzene-1,3-diyl)dimethanol is used as a key component in the production of specialty chemicals. Its versatility and potential for various applications make it an important compound in the synthesis of high-value specialty chemicals for different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6641-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6641-05:
(6*6)+(5*6)+(4*4)+(3*1)+(2*0)+(1*5)=90
90 % 10 = 0
So 6641-05-0 is a valid CAS Registry Number.
6641-05-0Relevant academic research and scientific papers
Efficient synthesis of (R)-ochratoxin alpha, the key precursor to the mycotoxin ochratoxin A
Lenz, Cesar Antonio,Rychlik, Michael
, p. 883 - 886 (2013/02/25)
Two new routes for the synthesis of enantiomerically pure ochratoxin alpha ((3R)-OTα) are presented, which is the key intermediate for the synthesis of ochratoxin A (OTA) by coupling reaction with the amino acid l-phenylalanine. The key step of both routes is the one pot directed ortho-metalation/alkylation/ lactonization of unprotected and suitably functionalized aromatic carboxylic acids, using lithium tetramethylpiperidide (LTMP) and (R)-propylene oxide.
