61265-06-3 Usage
Description
HERATOMIN is a dietary supplement that contains a blend of essential vitamins, minerals, and amino acids. It is formulated to support overall health and well-being by providing nutrients that may be missing in the diet. The key ingredients in HERATOMIN include vitamin A, vitamin C, vitamin D, vitamin E, vitamin K, B-complex vitamins, calcium, magnesium, zinc, selenium, and various essential amino acids. These nutrients play a crucial role in supporting immune function, promoting healthy skin and hair, maintaining proper muscle and bone function, and supporting overall energy levels. HERATOMIN is beneficial for individuals seeking to supplement their diet with essential nutrients to enhance their health and wellness.
Uses
Used in Health and Wellness Industry:
HERATOMIN is used as a dietary supplement for individuals looking to support their overall health and well-being. It provides essential nutrients that may be lacking in their diet, helping to maintain proper immune function, promote healthy skin and hair, support muscle and bone health, and enhance overall energy levels.
Used in Immune Function Support:
HERATOMIN is used as an immune function support supplement, providing essential vitamins and minerals that contribute to a healthy immune system. The blend of nutrients in HERATOMIN helps to strengthen the body's natural defenses against illness and infection.
Used in Skin and Hair Health:
HERATOMIN is used as a skin and hair health supplement, containing vitamins and minerals that promote healthy skin and hair growth. The nutrients in HERATOMIN support collagen production, skin hydration, and hair strength, contributing to a youthful and vibrant appearance.
Used in Muscle and Bone Health:
HERATOMIN is used as a muscle and bone health supplement, providing essential nutrients that support muscle growth and bone density. The vitamins and minerals in HERATOMIN contribute to maintaining proper muscle function and promoting strong, healthy bones.
Used in Energy Support:
HERATOMIN is used as an energy support supplement, providing essential B-complex vitamins and amino acids that help to convert food into energy. This helps to support overall energy levels and promote a more active and energetic lifestyle.
Check Digit Verification of cas no
The CAS Registry Mumber 61265-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,6 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61265-06:
(7*6)+(6*1)+(5*2)+(4*6)+(3*5)+(2*0)+(1*6)=103
103 % 10 = 3
So 61265-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O4/c1-10(2)5-7-18-13-9-11-3-4-14(17)20-15(11)12-6-8-19-16(12)13/h3-6,8-9H,7H2,1-2H3
61265-06-3Relevant articles and documents
Two Regiocomplementary Approaches to Angular Furanocoumarins with Chromium Carbene Complexes: Synthesis of Sphondin, Thiosphondin, Heratomin, and Angelicin
Wulff, William D.,McCallum, J. Stuart,Kunng, Fen-Ann
, p. 7419 - 7434 (2007/10/02)
Two regiocomplementary syntheses of the angular furanocoumarin sphondin are described utilizing the benzannulation reaction of furylcarbene complexes of chromium.The high regioselectivity of an intermolecular synthesis employing the reaction of pentacarbonylchromium (8) and methyl 4-pentynoate is thought to be controlled by the preferred conformation of an alkyne-carbene complex intermediate.By utilizing the same acetylene, heratomin and an unnatural derivative of sphondin, 6-methoxy-2-oxo(2H)-thiofuro(2,3-h)benzopyran were prepared from pentacarbonylchromium (37) and pentacarbonylchromium (31), respectively.An intramolecular synthesis of sphondin from oxy>carbene>pentacarbonylchromium (10e) incorporates the acetylene with reversed regiochemistry due to the geometrical constraints of the intramolecular annulation.Control over the formation of the regiochemistry correct for the carbon skeleton of sphondin is possible due to the regioselectivity in the annulation of unsymmetrical aromatic substituents (3-furyl) on the carbene carbon.The intramolecular synthesis is thus related to the intermolecular synthesis by a double reversal in the regiochemistry.A convergent synthesis of sphondin and angelicin is described which has the phenol 72 produced from the intramolecular benzannulation of complex 10e as a branch point and is differentiated by whether the phenol functionality is retained or reduced.
