콘텐츠로 건너뛰기
Merck
모든 사진(1)

주요 문서

모든 문서 보기

246050

Sigma-Aldrich

1,5-Cyclooctadiene

purified by redistillation, ≥99%

동의어(들):

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

로그인조직 및 계약 가격 보기
모든 사진(1)

About This Item

실험식(Hill 표기법):
C8H12
CAS Number:
111-78-4
Molecular Weight:
108.18
Beilstein:
2036542
EC Number:
203-907-1
MDL number:
MFCD00001752
UNSPSC 코드:
12352100
PubChem Substance ID:
24854773
NACRES:
NA.22

vapor pressure

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

Quality Level

100

분석

≥99%

양식

liquid

autoignition temp.

431 °F

정제법

redistillation

미포함

stabilizer

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

관련 카테고리

애플리케이션

1,5-Cyclooctadiene was used as a catalyst in the synthesis of aminoindene derivatives by the [3+2] annulation of ketimines with internal and terminal alkynes.

신호어

Danger

유해 및 위험 성명서

H226,H302 + H332,H304,H410

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

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
SHBR9071
SHBL6313
SHBJ2003
SHBF9503V
SHBG0583V

적합한 버전을 찾을 수 없으신가요?

특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Midori Nagamoto et al.
Chemical communications (Cambridge, England), 50(47), 6274-6277 (2014-05-07)
[3 + 2] Annulation of ketimines with internal and terminal alkynes proceeded via C-H activation to give aminoindene derivatives in high yields, which is catalyzed by a cationic iridium complex coordinated with 1,5-cyclooctadiene (cod).
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-

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

고객지원팀으로 연락바랍니다.