90921-11-2 Usage
Uses
Used in Pharmaceutical Industry:
Anemonin is used as a Chinese herbal medicinal ingredient for its ability to inhibit pigmentation synthesis in human melanocytes. This property makes it a potential candidate for the development of treatments for pigmentation disorders and hyperpigmentation conditions.
Used in Cosmetic Industry:
Due to its inhibitory effect on pigmentation synthesis, Anemonin can be used as an active ingredient in cosmetic products, such as skin lightening creams and lotions, to help reduce the appearance of dark spots, age spots, and uneven skin tone.
Used in Research:
Anemonin's biological activities and potential therapeutic effects make it a valuable compound for research purposes. It can be used in laboratory studies to investigate its mechanism of action, potential side effects, and possible applications in various medical and cosmetic fields.
Check Digit Verification of cas no
The CAS Registry Mumber 90921-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,2 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90921-11:
(7*9)+(6*0)+(5*9)+(4*2)+(3*1)+(2*1)+(1*1)=122
122 % 10 = 2
So 90921-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O4/c11-7-1-3-9(13-7)5-6-10(9)4-2-8(12)14-10/h1-4H,5-6H2/t9-,10-/m1/s1
90921-11-2Relevant articles and documents
STUDIES ON STRUCTURALLY SIMPLE α,β-BUTENOLIDES-I NEW SYNTHESIS OF RACEMIC γ-HYDROXYMETHYL-α,β-BUTENOLIDE AND DERIVATIVES
Cardellach, J.,Estopa, C.,Font, J.,Moreno-Manas, M.,Ortuno, R. M.,et al.
, p. 2377 - 2394 (2007/10/02)
Exhaustive approaches to the synthesis of racemic γ-heterosubstituted γ-methyl-α,β-butenolides are presented, starting from C3 synthons (glyceraldehyde, glycidaldehyde, acrolein and 2,3-epoxypropyl ethers).Good general methods for the preparation of γ-hydroxymethyl-α,β-butenolide 2, several of its ether derivatives, as well as of γ-bromomethyl-α,β-butenolide 5, are given.The reactivities of these structurally simple but highly functionalized compounds, convenient synthons for more complex molecules, are preliminarily explored.
