66582-32-9 Usage
Description
3-(Benzyloxy)-2,2-dimethylpropan-1-ol is an organic compound characterized by its benzyloxy and dimethylpropan-1-ol functional groups. It is a colorless liquid with a distinct aromatic odor and is known for its reactivity and stability in various chemical reactions.
Uses
Used in Chemical Synthesis:
3-(Benzyloxy)-2,2-dimethylpropan-1-ol is used as a protected intermediate for NPG Glycol (N897000), which is a key component in the synthesis of various organic compounds. Its protective nature allows for selective reactions, making it a valuable asset in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(Benzyloxy)-2,2-dimethylpropan-1-ol is used as a building block for the synthesis of complex drug molecules. Its unique structure and reactivity enable the creation of novel compounds with potential therapeutic applications.
Used in Tetraphenylporphyrin Synthesis:
3-(Benzyloxy)-2,2-dimethylpropan-1-ol is also utilized in the synthesis of tetraphenylporphyrins, which are important compounds in the field of materials science and have applications in areas such as solar energy conversion, catalysis, and molecular electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 66582-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,8 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66582-32:
(7*6)+(6*6)+(5*5)+(4*8)+(3*2)+(2*3)+(1*2)=149
149 % 10 = 9
So 66582-32-9 is a valid CAS Registry Number.
66582-32-9Relevant articles and documents
IMPROVED PROCESS FOR THE PREPARATION OF TEZACAFTOR INTERMEDIATE
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Page/Page column 11-12, (2021/03/05)
The present invention relates to an improved process for the preparation of tezacaftor intermediate compound of formula II. More particularly, the present invention relates to an improved, commercially viable process for the preparation of tezacaftor inte
Stereoselective Synthesis of γ-Butyrolactones Subunit of Polycavernoside A
Kadari, Sudhakar,Yerrabelly, Hemasri,Gogula, Thirupathi,Erukala, Yadaiah Goud,Yerrabelly, Jayaprakash Rao,Begari, Prem Kumar
, p. 1986 - 1990 (2018/08/01)
An efficient and versatile linear synthesis of γ-butyrolactone subunit of polycavernolide A has been reported in 14.2% overall yield with 10 linear steps by employing Sharpless asymmetric epoxidation, ring-closing metathesis, and diastereoface selective h
SUBSTITUTED TRICYCLICS AND METHOD OF USE
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Paragraph 1274, (2017/02/09)
The present invention provides for compounds of formula (I) wherein X, Y, and R1 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions mediated and modulated by CFTR, including cystic fibrosis, Sj?gren's syndrome, pancreatic insufficiency, chronic obstructive lung disease, and chronic obstructive airway disease. Also provided are pharmaceutical compositions comprised of one or more compounds of formula (I).