35984-93-1 Usage
General Description
2,9,16,23-Tetra-tert-butyl-29H,31H-phthalocyanine is a chemical compound that belongs to the phthalocyanine family. 2,9,16,23-TETRA-TERT-BUTYL-29H,31H-PHTHALOCYANINE is recognized for its unique properties including excellent thermal and chemical stability, high electron affinity, and resistance to oxidation. These characteristics make it useful in a broad array of applications in scientific and industrial fields. For instance, it's used as an active component in many electronic devices such as solar cells and gas sensors due to its excellent semiconducting properties, and in photodynamic therapy as a photosensitizer due to its ability to absorb light in the red and near-infrared region. Despite being highly soluble in organic solvents, it often exhibits low solubility in water which is generally improved by substituting the hydrogen atoms with tert-butyl groups.
Check Digit Verification of cas no
The CAS Registry Mumber 35984-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,8 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35984-93:
(7*3)+(6*5)+(5*9)+(4*8)+(3*4)+(2*9)+(1*3)=161
161 % 10 = 1
So 35984-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C48H48N8/c1-45(2,3)25-13-17-29-33(21-25)41-49-37(29)54-42-35-23-27(47(7,8)9)15-19-31(35)39(51-42)56-44-36-24-28(48(10,11)12)16-20-32(36)40(52-44)55-43-34-22-26(46(4,5)6)14-18-30(34)38(50-43)53-41/h13-24H,1-12H3/b53-38-,53-41-,54-37-,54-42-,55-40-,55-43-,56-39-,56-44-
35984-93-1Relevant articles and documents
THE SYNTHESES OF A MONOSUBSTITUTED AND AN UNSYMMETRICAL TETRASUBSTITUTED PHTHALOCYANINE USING BINUCLEAR PHTHALOCYANINES
Leznoff, Clifford C.,Greenberg, Shafrira
, p. 5555 - 5558 (1989)
The synthesis of 2-hydroxyphthalocyanine and 2-hydroxy-9,16,23-tri-tert-butylphthalocyanine have been accomplished.
