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Merck
모든 사진(1)

주요 문서

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475262

Sigma-Aldrich

1,3-Diiodobenzene

98%

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C6H4I2
CAS Number:
626-00-6
Molecular Weight:
329.90
EC Number:
210-921-1
MDL number:
MFCD00041731
UNSPSC 코드:
12352100
PubChem Substance ID:
24871105
NACRES:
NA.22

Quality Level

200

분석

98%

저장 조건

protect from light

mp

34-37 °C (lit.)

작용기

iodo

저장 온도

2-8°C

SMILES string

Ic1cccc(I)c1

InChI

1S/C6H4I2/c7-5-2-1-3-6(8)4-5/h1-4H

InChI key

SFPQFQUXAJOWNF-UHFFFAOYSA-N

일반 설명

1,3-Diiodobenzene is a halogenated benzene derivative. Its reaction with phenylboronic acid in the presence of CuI, DABCO (1,4-diazabicyclo[2.2.2]octane) and TBAB (n-Bu4NBr) has been analyzed. 1,3-Diiodobenzene undergoes coupling with 2-methylthiophene in the presence of Ir/Ag2CO3 to afford meta-linked isomer of thiophene-benzene-thiophene triad.

애플리케이션

1,3-Diiodobenzene may be used in the synthesis of:
  • 3,5-bis(perfluorodecyl)phenylboronic acid
  • epitaxially aligned and separated polyphenylene lines on Cu(110)
  • 1,3-bis(4-ethynyl-2,5-dibutoxyphenyl-1-ethynyl)benzene

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

235.4 °F - closed cup

Flash Point (°C)

113 °C - closed cup

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
BCCG0851
BCBX9230
BCBX5130
BCBW6665
BCBR6820V

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COA 검색

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Jin-Heng Li et al.
The Journal of organic chemistry, 72(6), 2053-2057 (2007-02-09)
In the presence of TBAB, CuI-catalyzed Suzuki-Miyaura cross-coupling of vinyl halides and aryl halides with arylboronic acids was conducted smoothly to afford the corresponding diarylethenes and polyaryls in moderate to good yields using DABCO (1,4-diazabicyclo[2.2.2]octane) as the ligand. We also
Benoît Join et al.
Angewandte Chemie (International ed. in English), 48(20), 3644-3647 (2009-04-09)
Efficient couplings using equimolar quantities of each coupling partner and multiple C-H bond arylation reactions are achieved with an Ir-based catalytic system for the C-H bond arylation of electron-rich heteroarenes with iodoarenes to construct extended pi-systems. The dramatic ligand effect
J A Lipton-Duffin et al.
Small (Weinheim an der Bergstrasse, Germany), 5(5), 592-597 (2009-02-26)
The surface-mediated synthesis of epitaxially aligned and separated polyphenylene lines on Cu(110) by exploiting the Ullmann dehalogenation reaction is reported. Scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS) show that the C-I bonds of 1,4-diiodobenzene and 1,3-diiodobenzene (C(6)H(4)I(2)) are
Synthesis, Chain Rigidity, and Luminescent Properties of Poly [(1, 3-phenyleneethynylene)-a lt-tris (2, 5-dialkoxy-1, 4-phenyleneethynylene)] s.
Chu Q, et al.
Macromolecules, 35(20), 7569-7574 (2002)
3, 5-Bis (perfluorodecyl) phenylboronic acid as an easily recyclable direct amide condensation catalyst.
Ishihara K, et al.
Synlett, 2001(09), 1371-1374 (2001)

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