Detail of > 876-53-9
- MSDS Download

- CAS Number:
- 876-53-9
- Name:
Tricyclo[3.3.1.13,7]decane,1,3-dibromo-
- Superlist Name:
- 1,3-Dibromoadamantane
- Formula:
- C10H14Br2
- Molecular Structure:
![Molecular Structure of 876-53-9 (Tricyclo[3.3.1.1<sup>3,7</sup>]decane,1,3-dibromo-)](http://www.lookchem.com/300w/2010/0626/876-53-9.jpg)
- Synonyms:
- Adamantane,1,3-dibromo- (6CI,7CI,8CI);NSC 102289;
- Molecular Weight:
- 294.03
- Density:
- 1.864 g/cm3
- Melting Point:
- 108-110 °C
- Boiling Point:
- 287.6 °C at 760 mmHg
- Flash Point:
- 145.4 °C
- Appearance:
- white solid
- Hazard Symbols:
Xi- Risk Codes:
- 36/37/38
- Safety:
- 26-36Details
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Reference
- Compositions for porous organic film with low dielectric constant
- Compositions for porous organic film with low dielectric constant. Satoh, Naoya; Yoshida, Yuji; Yokota, Akira (Sumitomo Chemical Company, Limited, Japan). U.S. Pat. Appl. Publ. US 2005025892 A1 3 Feb 2005, 15 pp. (English). (United States of America). CODEN: USXXCO. CLASS: ICM: B05D003-02. APPLICATION: US 2003-694400 28 Oct 2003. PRIORITY: JP 2002-319508 1 Nov 2002; JP 2003-180648 25 Jun 2003. DOCUMENT TYPE: Patent CA Section: 38 (Plastics Fabrication and Uses) Section cross-reference(s): 76 The present invention provides a compn. comprising (A) 31 selected from an arom. polymer having a repeating unit I and a monomer having 32 CYCH groups and (B) 31 selected from a heat transpirable compd.In this article, certain chemicals are used. Some of their cas registry numbers are 600736-93-4 and 876-53-9 and a heat decomposable compd., wherein Ar1 = (substituted) arom. ring excluding CYCH substituent; X1, X2 = direct bond, (substituted) C1-20 alkylene, CR1:CR2, CYC, (substituted) divalent group having an arom. ring, (substituted) divalent group having alicyclic hydrocarbob ring, O, CO, COO, S, SO, SO2, NR3, or CONR4; R1, R2, R3, R4 = H or (substituted) C1-20 alkyl or alkoxy, (substituted) C4-20 alicyclic hydrocarbon, (substituted) aryl; Y1 = divalent org. group; and n = 31 integer. Thus, 9.6 g 9,9-bis(4-dihydroxyphenyl)fluorene and 5.4 g 1-(trimethylsilylethynyl)-2,4-difluorobenzene were reacted at 120° for 12 h, at 130° for 2 h, and at 150° for 4 h to give a copolymer with wt. av. mol. wt. 7600, 65 parts of which was mixed with 35 parts a-methylstyrene homopolymer with wt. av. mol. wt. 4600 in anisole, applied on a silicon wafer, baked at 150° for 1 min and 400° for 30 min to give a test piece with dielec. const. 2.35. .
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