추천 제품
분석
98%
형태
solid
mp
>300 °C (lit.)
SMILES string
c1ccc(cc1)-c2c(-c3ccccc3)c(-c4ccccc4)c(-c5ccccc5)c(-c6ccccc6)c2-c7ccccc7
InChI
1S/C42H30/c1-7-19-31(20-8-1)37-38(32-21-9-2-10-22-32)40(34-25-13-4-14-26-34)42(36-29-17-6-18-30-36)41(35-27-15-5-16-28-35)39(37)33-23-11-3-12-24-33/h1-30H
InChI key
QBHWPVJPWQGYDS-UHFFFAOYSA-N
애플리케이션
Hexaphenylbenzene can be used as a starting material to synthesize:
- 1,2,3,4,5,6-Hexacyclohexylcyclohexane by Pd/C catalyzed hydrogenation reaction.
- Stable hexatrityl cations and porous organic polymers for applications in catalysis and gas storage.
- Hexa-peri-hexabenzocoronene via one-pot substitution and oxidative cyclodehydrogenation reaction in the presence of t-BuCl/FeCl3.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Porous organic polymers based on propeller-like hexaphenylbenzene building units
Macromolecules, 44(14), 5573-5577 (2011)
From Hexaphenylbenzene to 1,2,3,4,5,6-Hexacyclohexylcyclohexane
Journal of the American Chemical Society, 142(30), 12916-12920 (2020)
Chemical communications (Cambridge, England), 49(9), 895-897 (2012-12-19)
Fluorescent nanorods formed by self-assembly of hexaphenylbenzene derivative in the presence of cyanide ions serve as a sensitive colorimetric and fluorogenic sensor for the detection of trinitrotoluene (TNT) at the attogram (10(-18) g) level with a detection limit of 10.21
Synthesis and isolation of polytrityl cations by utilizing hexaphenylbenzene and tetraphenylmethane scaffolds
The Journal of Organic Chemistry, 69(5), 1524-1530 (2004)
A Practical One-Pot Synthesis of Soluble Hexa-peri-hexabenzocoronene and Isolation of Its Cation-Radical Salt
J. Org. React., 68(10), 4071-4074 (2003)
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