6256-31-1 Usage
Uses
Used in Cosmetic and Personal Care Products:
o-Chloro-alpha,alpha-dimethylphenethyl alcohol is used as a preservative for its ability to prevent the growth of microorganisms, ensuring the longevity and safety of cosmetic and personal care products.
Used in Skincare Products:
o-Chloro-alpha,alpha-dimethylphenethyl alcohol is used as an antiseptic and anti-inflammatory agent for its mild properties that help soothe and protect the skin, making it suitable for skincare formulations.
Used in Muscle Relaxant Products:
o-Chloro-alpha,alpha-dimethylphenethyl alcohol is used as a muscle relaxant for its properties that help relieve muscle tension and pain, making it a beneficial component in products designed for muscle relaxation and pain relief.
If there are additional applications in different industries, they can be listed as follows:
Used in Pharmaceutical Industry:
o-Chloro-alpha,alpha-dimethylphenethyl alcohol is used as an active pharmaceutical ingredient for its potential therapeutic effects, such as its antiseptic, anti-inflammatory, and muscle-relaxing properties.
Used in Food Preservation:
o-Chloro-alpha,alpha-dimethylphenethyl alcohol is used as a preservative in the food industry to extend the shelf life of products by inhibiting the growth of bacteria and other microorganisms.
Check Digit Verification of cas no
The CAS Registry Mumber 6256-31-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6256-31:
(6*6)+(5*2)+(4*5)+(3*6)+(2*3)+(1*1)=91
91 % 10 = 1
So 6256-31-1 is a valid CAS Registry Number.
6256-31-1Relevant academic research and scientific papers
Pd(II)-catalyzed hydroxyl-directed C-H olefination enabled by monoprotected amino acid ligands
Lu, Yi,Wang, Dong-Hui,Engle, Keary M.,Yu, Jin-Quan
supporting information; experimental part, p. 5916 - 5921 (2010/07/05)
A novel Pd(II)-catalyzed ortho-C-H olefination protocol has been developed using spatially remote, unprotected tertiary, secondary, and primary alcohols as the directing groups. Mono-N-protected amino acid ligands were found to promote the reaction, and an array of olefin coupling partners could be used. When electron-deficient alkenes were used, the resulting olefinated intermediates underwent subsequent Pd(II)-catalyzed oxidative intramolecular cyclization to give the corresponding pyran products, which could be converted into ortho-alkylated alcohols under hydrogenolysis conditions. The mechanistic details of the oxidative cyclization step are discussed and situated in the context of the overall catalytic cycle.
