76-35-7 Usage
Uses
Used in Chemical Synthesis:
2,2-Dimethyl-1,3-butanediol is used as a synthetic intermediate for the production of various chemicals, contributing to the creation of a wide range of compounds that serve different industries.
Used as a Solvent:
In the chemical industry, 2,2-Dimethyl-1,3-butanediol is utilized as a solvent, leveraging its ability to dissolve a variety of substances, which is crucial for numerous chemical processes and reactions.
Used in Alternative Fuels:
2,2-Dimethyl-1,3-butanediol is used as a potential alternative to traditional fossil fuels due to its renewable and sustainable nature, offering an environmentally friendly option for energy production.
Used in Personal Care Products:
2,2-Dimethyl-1,3-butanediol is used as an ingredient in certain personal care products, taking advantage of its antimicrobial properties to enhance the products' efficacy and safety.
Used in Pharmaceuticals:
In the pharmaceutical industry, 2,2-Dimethyl-1,3-butanediol is used for its antimicrobial properties, playing a role in the development of treatments and medications that require such characteristics.
Used in Antimicrobial Applications:
2,2-Dimethyl-1,3-butanediol is employed for its antimicrobial properties, serving as an effective agent against various microorganisms, which is beneficial in both personal care and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 76-35-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76-35:
(4*7)+(3*6)+(2*3)+(1*5)=57
57 % 10 = 7
So 76-35-7 is a valid CAS Registry Number.
76-35-7Relevant articles and documents
Methylation-ring opening of 3,3-disubstituted 2,3-epoxy alcohols. Synthesis of chiral quaternary fragments for assembly of briaran diterpenes
Balasubramaniam, Rajiv P.,Moss, David K.,Wyatt, Justin K.,Spence, John D.,Gee, Arvin,Nantz, Michael H.
, p. 7429 - 7444 (2007/10/03)
Two chiral quaternary carbon-containing fragments suitable for elaboration to the briaran diterpenes were obtained by regioselective methylation of functionalized 3,3-disubstituted 2,3-epoxy-1-ols. The factors which favor methylation at the more hindered position of a trisubstituted 2,3-epoxy alcohol were determined.
