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Merck
CN

V2208

Sigma-Aldrich

4-乙烯基-1-环己烯

99%

别名:

4-乙烯基-1-环己烯, 神经干细胞 15760

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About This Item

线性分子式:
C6H9CH=CH2
CAS号:
分子量:
108.18
Beilstein:
1901553
EC 号:
MDL编号:
UNSPSC代码:
12162002
PubChem化学物质编号:

蒸汽密度

3.76 (vs air)

蒸汽压

10.2 mmHg ( 25 °C)

方案

99%

自燃温度

517 °F

包含

25-200 ppm p-tert-butylcatechol as inhibitor

折射率

n20/D 1.463 (lit.)

沸点

126-127 °C (lit.)

mp

−101 °C (lit.)

密度

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

储存温度

2-8°C

SMILES字符串

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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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

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
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
J K Doerr-Stevens et al.
Drug metabolism and disposition: the biological fate of chemicals, 27(2), 281-287 (1999-02-04)
4-Vinylcyclohexene (VCH), an ovarian toxicant in mice, is known to irreversibly deplete ovarian follicles as a consequence of VCH diepoxide formation. Because ovotoxicity requires repeated dosing of VCH, the effect of consecutive daily doses of VCH (7.5 mmol/kg/day) on mouse

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