834895-46-4 Usage
Description
Pyrrolidine, 1-[2-methyl-4-(3-phenyl-3H-naphtho[2,1-b]pyran-3-yl)phenyl]is a complex organic molecule with a pyrrolidine backbone and a substituted phenyl group. The molecule contains a fused naphthopyran ring system with a phenyl substitution at the 3-position. It also has a 2-methyl-4-phenyl substitution on the other phenyl group. This unique structure and properties may have potential pharmaceutical or industrial applications, but further research would be needed to fully understand its properties and potential uses.
Uses
Used in Pharmaceutical Industry:
Pyrrolidine, 1-[2-methyl-4-(3-phenyl-3H-naphtho[2,1-b]pyran-3-yl)phenyl]may be used as a pharmaceutical compound for the development of new drugs due to its unique structure and properties. Its potential applications could include the treatment of various diseases and conditions, but further research would be needed to fully understand its therapeutic potential.
Used in Chemical Industry:
Pyrrolidine, 1-[2-methyl-4-(3-phenyl-3H-naphtho[2,1-b]pyran-3-yl)phenyl]may also have potential applications in the chemical industry, such as in the synthesis of other complex organic molecules or as a component in various chemical processes. Its unique structure and properties could make it a valuable building block for the development of new materials and compounds. However, further research would be needed to fully explore its potential applications in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 834895-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,4,8,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 834895-46:
(8*8)+(7*3)+(6*4)+(5*8)+(4*9)+(3*5)+(2*4)+(1*6)=214
214 % 10 = 4
So 834895-46-4 is a valid CAS Registry Number.
834895-46-4Relevant articles and documents
Synthesis and photochromic properties of substituted 3H-naphtho[2,1-b] pyrans
Gabbutt, Christopher D.,Heron, B. Mark,Instone, Alicia C.,Horton, Peter N.,Hursthouse, Michael B.
, p. 463 - 471 (2007/10/03)
The synthesis and spectroscopic properties of novel 3H-naphtho[2,1-b]pyrans are described. Subtle variation of the colour of the photo-generated merocyanine dyes derived from these naphthopyrans can be accomplished by controlling the steric interactions between a terminal pyrrolidine donor group and a proximal substituent.
