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CIS-STILBENE

CIS-STILBENE Structure
CAS No.
645-49-8
Chemical Name:
CIS-STILBENE
Synonyms
Stilbebe;Nsc66424;ISOSTILBENE;CIS-BIBENZAL;CIS-STILBEBE;CIS-STILBENE;(Z)-Stilbene;Dibenzal(cis);CIS-TOLUYLENE;(αZ)-Stilbene
CBNumber:
CB8211190
Molecular Formula:
C14H12
Molecular Weight:
180.25
MOL File:
645-49-8.mol
MSDS File:
SDS
Modify Date:
2023/12/26 11:30:52

CIS-STILBENE Properties

Melting point -5°C
Boiling point 82-84 °C0.4 mm Hg(lit.)
Density 1.011 g/mL at 25 °C(lit.)
refractive index n20/D 1.622(lit.)
Flash point >230 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Yellow to Green
Water Solubility Immiscible with water. Miscible with ethanol.
Merck 14,8817
BRN 1616739
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
LogP 4.830 (est)
CAS DataBase Reference 645-49-8(CAS DataBase Reference)
EPA Substance Registry System cis-Stilbene (645-49-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/38
Safety Statements  26-36
WGK Germany  3
RTECS  DA0513600
HS Code  29029090
NFPA 704
0
0 0

CIS-STILBENE price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S4808 cis-Stilbene 96% 645-49-8 1G ₹1941.98 2022-06-14 Buy
Sigma-Aldrich(India) S4808 cis-Stilbene 96% 645-49-8 5G ₹8928.98 2022-06-14 Buy
Sigma-Aldrich(India) S4808 cis-Stilbene 96% 645-49-8 10G ₹15402.23 2022-06-14 Buy
ALFA India ALF-A11924-14 cis-Stilbene, 97% 645-49-8 25g ₹28608 2022-05-26 Buy
TCI Chemicals (India) S0089 cis-Stilbene min. 96.0 % 645-49-8 1ML ₹1800 2022-05-26 Buy
Product number Packaging Price Buy
S4808 1G ₹1941.98 Buy
S4808 5G ₹8928.98 Buy
S4808 10G ₹15402.23 Buy
ALF-A11924-14 25g ₹28608 Buy
S0089 1ML ₹1800 Buy

CIS-STILBENE Chemical Properties,Uses,Production

Chemical Properties

pale yellow liquid

Uses

cis-Stilbene: stilbene and its natural derivatives such as resveratrol and vitisins inhibits Staphylococcus aureus hemolytic activity and biofilm formation without affecting its bacterial growth

General Description

Oily yellow liquid. Freezing point 5°C. Insoluble in water. Soluble in ethanol. Unstable relative to the trans isomer, which is a solid with a melting point of 122-124°C.

Air & Water Reactions

Sensitive to prolonged exposure to air and light [Lancaster]. Insoluble in water.

Reactivity Profile

CIS-STILBENE may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release gaseous hydrogen.

Fire Hazard

Flash point data for CIS-STILBENE are not available, however CIS-STILBENE is probably combustible.

Purification Methods

Purify it by chromatography on alumina using hexane and distil it under vacuum. (The final product contains ca 0.1% of the trans-isomer.) [Lewis et al. J Am Chem Soc 107 203 1985, Saltiel J Phys Chem 91 2755 1987, Beilstein 5 H 630.]

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(1,2-Ethenediyl)-1,1-bisbenzene, (Z)- (Z)-1,2-Diphenylethene (Z)-1,2-Diphenylethylene [(Z)-2-Phenylethenyl]benzene 1,1’-(1,2-ethenediyl)bis-,(Z)-Benzene 1,2-Diphenylethene, (Z)- 1,cis-2-Diphenylethene 1,cis-2-Diphenylethylene 1’-(1,2-ethenediyl)bis-(z)-benzen Benzene, 1,1'-(1,2-ethenediyl)bis-, (Z)- Benzene, 1,1'-(1,2-ethenedyl)bis-, (Z)- benzene,1,1’-(1,2-ethenediyl)bis-,(Z)- cis-1,2-Diphenylethene cis-1,2-diphenyl-ethene cis-Diphenylethene cis-Diphenylethylene Dibenzal(cis) Dibenzilidene(cis) ethene,1,2-diphenyl-,cis- Stilbene, (Z)- CIS-BIBENZAL CIS-BIBENZYLIDENE CIS-A B-DIPHENYLETHYLENE CIS-STILBEBE CIS-STILBENE CIS-TOLUYLENE CIS-1,2-DIPHENYLETHYLENE cis-1,1-(1,2-Ethenediyl)bis(benzene) Stilbebe ISOSTILBENE cis-Stilbene,97% Benzene, 1,1-(1Z)-1,2-ethenediylbis- cis-1,2-Diphenylethylene, Isostilbene (Z)-Stilbene (αZ)-Stilbene [(Z)-Ethene-1,2-diyl]bisbenzene 1,1'-[(Z)-1,2-Ethenediyl]bisbenzene Nsc66424 cis-stilbene anion radical cis-Stilbene 96% cis-Stilbene > CIS-STILBENE ISO 9001:2015 REACH 645-49-8 C6H5CHCHC6H5 645498 C14H12 Stilbenes Building Blocks Alkenes Acyclic Organic Building Blocks Acyclic Alkenes Bioactive Small Molecules Building Blocks Cell Biology Chemical Synthesis Organic Building Blocks