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Merck
모든 사진(4)

주요 문서

C109207

Sigma-Aldrich

1,5-Cyclooctadiene

contains 50-150 ppm 4-tert-Butylcatechol, 99%

동의어(들):

1,5-COD, cis-1,5-Cyclooctadiene, COD

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About This Item

실험식(Hill 표기법):
C8H12
CAS Number:
Molecular Weight:
108.18
Beilstein:
2036542
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

25.8 mmHg ( 37.7 °C)
6.8 mmHg ( 25 °C)

Quality Level

분석

99%

양식

liquid

autoignition temp.

431 °F

포함

50-150 ppm 4-tert-Butylcatechol as stabilizer
50-150 ppm 4-tert-Butylcatechol

refractive index

n20/D 1.493 (lit.)

bp

149-150 °C (lit.)

mp

−69 °C (lit.)

density

0.882 g/mL at 25 °C (lit.)

SMILES string

C1CC=CCCC=C1

InChI

1S/C8H12/c1-2-4-6-8-7-5-3-1/h1-2,7-8H,3-6H2/b2-1-,8-7-

InChI key

VYXHVRARDIDEHS-QGTKBVGQSA-N

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애플리케이션

  • Bis(Aluminyl)Magnesium: A Source of Nucleophilic or Radical Aluminium-Centred Reactivity.: Investigates 1,5-Cyclooctadiene′s ability to stabilize reactive intermediates in metal complexes, which is crucial for developing new pharmaceutical agents and enhancing ligand efficiency in transition metal catalysis (Griffin et al., 2024).

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

100.4 °F - closed cup

Flash Point (°C)

38 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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시험 성적서(COA)

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문서 라이브러리 방문

Eleonora Cavallari et al.
The journal of physical chemistry. B, 119(31), 10035-10041 (2015-07-15)
Hyperpolarization of (13)C carboxylate signals of metabolically relevant molecules, such as acetate and pyruvate, was recently obtained by means of ParaHydrogen Induced Polarization by Side Arm Hydrogenation (PHIP-SAH). This method relies on functionalization of the carboxylic acid with an unsaturated
Adrian Tlahuext-Aca et al.
Dalton transactions (Cambridge, England : 2003), 43(42), 15997-16005 (2014-09-19)
Ni(0)-catalyzed dehydrogenation of benzylic-type imines was performed to yield asymmetrical tetra-substituted imidazoles and 2-imidazolines. This was achieved with a single operational step while maintaining good selectivity and atom economy. The catalytic system shows low to moderate tolerance for fluoro-, trifluoromethyl-

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