488-66-4 Usage
Uses
Used in Dietary Supplements:
2,3,4,5,6-Pentahydroxycyclohexan-1-one is used as a dietary supplement for its essential role in maintaining overall health. It helps in the synthesis of collagen, promoting skin, bone, and connective tissue health, and supports the immune system's proper functioning.
Used in Food and Beverage Industry:
2,3,4,5,6-Pentahydroxycyclohexan-1-one is used as a nutritional enhancer in various foods and beverages. Its addition improves the nutritional value of these products, providing consumers with the health benefits of vitamin C, such as antioxidant protection and enhanced iron absorption.
Used in Pharmaceutical Industry:
2,3,4,5,6-Pentahydroxycyclohexan-1-one is used in the pharmaceutical industry for its therapeutic applications. It is employed in the treatment of various conditions, including scurvy, a disease caused by vitamin C deficiency, and in wound healing due to its role in collagen synthesis.
Used in Cosmetic Industry:
2,3,4,5,6-Pentahydroxycyclohexan-1-one is used in the cosmetic industry for its skin health benefits. It is incorporated into skincare products for its antioxidant properties, promoting collagen synthesis and providing protection against environmental stressors that can cause skin damage.
Check Digit Verification of cas no
The CAS Registry Mumber 488-66-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 488-66:
(5*4)+(4*8)+(3*8)+(2*6)+(1*6)=94
94 % 10 = 4
So 488-66-4 is a valid CAS Registry Number.
488-66-4Relevant academic research and scientific papers
Protecting group directed stereoselective reduction of an epi-inosose: Efficient synthesis of epi-inositol
Patil, Madhuri T.,Krishnaswamy, Shobhana,Sarmah, Manash P.,Shashidhar, Mysore S.
supporting information; experimental part, p. 3756 - 3758 (2011/08/06)
A facile and high yielding synthesis of epi-inositol via stereoselective reduction of a pentaprotected epi-inosose is reported. Extent of stereoselectivity during the hydride reduction appears to depend on the ability of the substrate to complex with metal ions in the reducing agent.
