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Merck
모든 사진(1)

Key Documents

52985

Sigma-Aldrich

cis-3-Hexene

≥95.0%

로그인조직 및 계약 가격 보기


About This Item

실험식(Hill 표기법):
C6H12
CAS Number:
Molecular Weight:
84.16
Beilstein:
1718858
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

≥95.0%

refractive index

n20/D 1.395

bp

66-68 °C (lit.)

density

0.681 g/mL at 20 °C (lit.)

SMILES string

CC\C=C/CC

InChI

1S/C6H12/c1-3-5-6-4-2/h5-6H,3-4H2,1-2H3/b6-5-

InChI key

ZQDPJFUHLCOCRG-WAYWQWQTSA-N

일반 설명

cis-3-Hexene is a symmetrical cis-disubstituted alkene that can be prepared by the hydroboration of 3-hexyne followed by protonolysis. The gas-phase study of its molecular structure by electron diffraction combined with molecular mechanical calculations reveals the presence of the (+ac, +ac) and the (-ac, +ac) forms. cis-3-Hexene undergoes epoxidation with dimethyldioxirane to form the corresponding epoxide.

애플리케이션

cis-3-Hexene may be used in the preparation of 3-hexanol via asymmetric hydroboration with diisopinocampheylborane (Ipc2BH).

픽토그램

FlameHealth hazardExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

-13.0 °F - closed cup

Flash Point (°C)

-25 °C - closed cup

개인 보호 장비

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


시험 성적서(COA)

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문서 라이브러리 방문

The molecular structures of cis-3-hexene and trans-3-hexene in the gas phase by electron diffraction and molecular mechanical calculations.
Van HD, et al.
Journal of Molecular Structure, 74(1), 123-135 (1981)
Epoxidation by dimethyldioxirane. Electronic and steric effects.
Baumstark AL and Vasquez PC.
The Journal of Organic Chemistry, 53(15), 3437-3439 (1988)
Hydroboration. XI. The hydroboration of acetylenes-A convenient conversion of internal acetylenes into cis-olefins and of terminal acetylenes into aldehydes
Brown HC and Zweifel G.
Journal of the American Chemical Society, 83(18), 3834-3840 (1961)
Hydroboration. 61. Diisopinocampheylborane of high optical purity. Improved preparation and asymmetric hydroboration of representative cis-disubstituted alkenes.
Brown HC, et al.
The Journal of Organic Chemistry, 47(26), 5065-5069 (1982)
Nadhem Aissani et al.
Journal of agricultural and food chemistry, 63(27), 6120-6125 (2015-06-18)
Research on new pesticides based on plant extracts, aimed at the development of nontoxic formulates, has recently gained increased interest. This study investigated the use of the volatilome of rucola (Eruca sativa) as a powerful natural nematicidal agent against the

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