Merck
CN

94950

Supelco

4-乙烯基-1-环己烯

analytical standard

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别名:
4-乙烯基-1-环己烯, 神经干细胞 15760
线性分子式:
C6H9CH=CH2
CAS号:
分子量:
108.18
Beilstein:
1901553
EC 号:
MDL编号:
PubChem化学物质编号:

等级

analytical standard

质量水平

蒸汽密度

3.76 (vs air)

蒸汽压

10.2 mmHg ( 25 °C)

检测方案

≥99.5% (GC)

自燃温度

517 °F

保质期

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.463 (lit.)
n20/D 1.464

bp

126-127 °C (lit.)

mp

−101 °C (lit.)

密度

0.831 g/mL at 20 °C
0.831 g/mL at 20 °C
0.832 g/mL at 25 °C (lit.)

application(s)

environmental
petroleum

格式

neat

储存温度

2-8°C

SMILES string

C=CC1CCC=CC1

InChI

1S/C8H12/c1-2-8-6-4-3-5-7-8/h2-4,8H,1,5-7H2

InChI key

BBDKZWKEPDTENS-UHFFFAOYSA-N

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1 of 4

此商品
440282892068450
4-Vinyl-1-cyclohexene analytical standard

Supelco

94950

4-乙烯基-1-环己烯

Cyclohexene analytical standard, ≥99.5% (GC)

Supelco

44028

环己烯

Cyclohexane analytical standard

Supelco

28920

环己烷

2-Methyl-1-pentene analytical standard

Supelco

68450

2-甲基-1-戊烯

assay

≥99.5% (GC)

assay

≥99.5% (GC)

assay

≥99.7% (GC)

assay

≥99.0% (GC)

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

environmental
petroleum

application(s)

environmental
petroleum

application(s)

environmental

application(s)

environmental
petroleum

format

neat

format

neat

format

neat

format

neat

一般描述

4-乙烯基-1-环己烯可以在亚硝酰基铁催化剂如[Fe(NO)2(CO)2] 或 [{FeCl(NO)2}2]/还原剂的存在下通过丁二烯的环二聚化合成。

应用

有关合适的仪器技术的更多信息,请参阅产品′的检验报告。想要获得更多支持,请联系技术服务部。

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

警示用语:

Danger

危险分类

Aquatic Chronic 3 - Asp. Tox. 1 - Carc. 2 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

60.8 °F - closed cup

闪点(°C)

16 °C - closed cup

个人防护装备

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

法规信息

危险化学品

分析证书(COA)

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T1503
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Sigma-Aldrich

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亚甲基环己烷

Inorganic Reactions and Methods, Reactions Catalyzed by Inorganic Compounds (2009)
D A Keller et al.
Toxicology and applied pharmacology, 144(1), 36-44 (1997-05-01)
4-Vinylcyclohexene (4-VCH), the dimer of 1,3-butadiene, is an ovarian toxicant in mice due to the formation of a diepoxide metabolite, but the tissue-specific site of formation of the metabolites is unknown. Microsomal preparations from liver, lung, and ovaries obtained from
Gold(I)-catalyzed asymmetric cycloisomerization of eneallenes into vinylcyclohexenes.
Michael A Tarselli et al.
Angewandte Chemie (International ed. in English), 46(35), 6670-6673 (2007-07-31)
Patricia B Hoyer et al.
Birth defects research. Part B, Developmental and reproductive toxicology, 80(2), 113-125 (2007-03-08)
The occupational chemical 4-vinylcyclohexene (VCH) has been shown to cause destruction of small pre-antral follicles in ovaries of mice. Further, its monoepoxide metabolites, 1,2-VCH epoxide, 7,8-VCH epoxide, and the diepoxide, VCD, have been shown to cause pre-antral follicle loss in
Cinzia Chiappe et al.
Chemical research in toxicology, 16(1), 56-65 (2003-04-16)
The stereochemical course of the biotransformation of 1,2-monoepoxides of 4-vinylcyclohexene (2 and 3) by liver microsomes from control and induced rats and by purified P4502B1 and P4502E1 has been determined. The epoxidation of monoexpodies cis-4-vinylcyclohexene 1,2-epoxide (2) and trans-4-vinylcyclohexene 1,2-epoxide

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