1821816-32-3 Usage
Uses
Used in Pharmaceutical Research:
(+)-(1S,2S)-2-(3,5-dimethylphenyl)cyclopropylmethanol is used as a building block in pharmaceutical research for the development of molecules with targeted biological activities. Its unique structure allows for the creation of compounds that can potentially address various medical conditions.
Used in Chemical Synthesis:
In the field of chemical synthesis, (+)-(1S,2S)-2-(3,5-dimethylphenyl)cyclopropylmethanol is employed as a key intermediate for synthesizing complex organic compounds. Its chiral nature and cyclopropane ring provide a versatile platform for the construction of a wide range of molecules.
Used in Pain Management:
(+)-(1S,2S)-2-(3,5-dimethylphenyl)cyclopropylmethanol has been studied for its potential anti-inflammatory and analgesic properties, making it a candidate for the development of new drugs aimed at pain management. Further research is necessary to fully understand its pharmacological potential and any associated risks.
Used in Medical Condition Treatment:
Due to its potential biological activities, (+)-(1S,2S)-2-(3,5-dimethylphenyl)cyclopropylmethanol may find applications in the treatment of various medical conditions. Its development into new drugs could offer novel therapeutic options for patients in need. However, additional research is required to validate its efficacy and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 1821816-32-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,2,1,8,1 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1821816-32:
(9*1)+(8*8)+(7*2)+(6*1)+(5*8)+(4*1)+(3*6)+(2*3)+(1*2)=163
163 % 10 = 3
So 1821816-32-3 is a valid CAS Registry Number.
1821816-32-3Relevant academic research and scientific papers
Catalytic asymmetric cyclopropanation of allylic alcohols with titanium-TADDOLate: Scope of the cyclopropanation reaction
Charette,Molinaro,Brochu
, p. 12168 - 12175 (2007/10/03)
A substoichiometric amount of titanium-TADDOLate complex was effective at catalyzing the cyclopropanation reaction of allylic alcohols in the presence 1 equiv of bis(iodomethyl) zinc. After initial optimization of the catalyst structure, excellent yields and enantiomeric ratios were obtained for 3-aryl- or 3-heteroaryl-substituted allylic alcohols (up to 97:3). Alkyl-substituted allylic alcohols gave modest yields and enantiomeric ratios (up to 87:13) but these compare favorably with those observed with other substoichiometric chiral ligands. The full synthetic scope of the reaction is presented in this paper.
