92396-88-8 Usage
Description
BIS(TRIHEXYLSILOXY)SILICON 2,3-NAPH-THALOCYANINE is a light-induced crosslinkable semiconducting polymer dot that exhibits unique properties, making it a valuable compound in various applications.
Uses
Used in Biomedical Applications:
BIS(TRIHEXYLSILOXY)SILICON 2,3-NAPH-THALOCYANINE is used as a cell imaging agent for its ability to provide high-resolution imaging and efficient labeling of cells.
Used in Pharmaceutical Industry:
BIS(TRIHEXYLSILOXY)SILICON 2,3-NAPH-THALOCYANINE is used as a drug delivery system for its potential to improve the targeting and efficiency of drug delivery, enhancing therapeutic outcomes.
Used in Material Science:
BIS(TRIHEXYLSILOXY)SILICON 2,3-NAPH-THALOCYANINE is used as a semiconducting material for its unique electronic properties, which can be utilized in the development of advanced electronic devices and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 92396-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,9 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92396-88:
(7*9)+(6*2)+(5*3)+(4*9)+(3*6)+(2*8)+(1*8)=168
168 % 10 = 8
So 92396-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C48H24N8.2C18H39OSi.Si/c1-2-10-26-18-34-33(17-25(26)9-1)41-49-42(34)54-44-37-21-29-13-5-6-14-30(29)22-38(37)46(51-44)56-48-40-24-32-16-8-7-15-31(32)23-39(40)47(52-48)55-45-36-20-28-12-4-3-11-27(28)19-35(36)43(50-45)53-41;2*1-4-7-10-13-16-20(19,17-14-11-8-5-2)18-15-12-9-6-3;/h1-24H;2*4-18H2,1-3H3;/q-2;2*-1;+4
92396-88-8Relevant articles and documents
PREPARATION OF SILICON PHTHALOCYANINES AND GERMANIUM PHTHALOCYANINES AND RELATED SUBSTANCES
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Page/Page column 16-17, (2010/05/13)
A process for preparing compounds of the general formula (I) by reacting the compound of the general formula (II) where L, L′ are the same or different and are each independently Cl or OH in the presence of a. chlorine compounds Cl-M2R1R2R3, Cl-M3R4R5R6, with the proviso that L and L′ are not both simultaneously OH, or b. hydroxyl compounds HO-M2R1R2R3, HO-M3R4R5R6. The use of compounds of the general formula (I) as markers for liquids and a process for detecting markers in liquids.