61265-06-3

Basic information

• Product Name: HERATOMIN
• Synonyms: HERATOMIN;6-[(3-Methyl-2-butenyl)oxy]-2H-furo[2,3-h]-1-benzopyran-2-one;6-[(3-Methyl-2-buten-1-yl)oxy]-2H-furo[2,3-h]-1-benzopyran-2-one
• CAS NO: 61265-06-3
• Molecular Formula: C16H14O4
• Molecular Weight: 270.28
• Mol File: 61265-06-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 448.3°Cat760mmHg
• Flash Point: 224.9°C
• Appearance: /
• Density: 1.242
• Vapor Pressure: 3.13E-08mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: HERATOMIN(CAS DataBase Reference)
• NIST Chemistry Reference: HERATOMIN(61265-06-3)
• EPA Substance Registry System: HERATOMIN(61265-06-3)

Safety Data

• Hazardous Substances Data: 61265-06-3(Hazardous Substances Data)

Usage

General Description

HERATOMIN is a dietary supplement that contains a blend of vitamins, minerals, and amino acids. It is designed to support overall health and well-being by providing essential nutrients that may be lacking 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 are important for supporting immune function, promoting healthy skin and hair, maintaining proper muscle and bone function, and supporting overall energy levels. HERATOMIN may be beneficial for individuals looking to supplement their diet with essential nutrients to support overall health and wellness.

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

Upstream product

• 116663-81-1 6-(3-methyl-2-butenoxy)-2-oxo-(2,3,4H)-furo<2,3-h><1>benzopyran 

Relevant articles and documents

Two Regiocomplementary Approaches to Angular Furanocoumarins with Chromium Carbene Complexes: Synthesis of Sphondin, Thiosphondin, Heratomin, and Angelicin

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.