Meso Stilbene Dibromide Boiling Point

Organic molecule

meso-Stilbene dibromide

Names
Preferred IUPAC proper noun 1,one′-[(1R,iiDue south)-1,2-Dibromoethane-1,two-diyl]dibenzene
Other names Stilbene dibromide; meso-one,2-dibromo-one,2-diphenyl ethane
Identifiers
CAS Number	13440-24-nine
3D model (JSmol)	Interactive paradigm
ChEMBL	ChEMBL3115205
ChemSpider	2279317
ECHA InfoCard	100.162.977
PubChem CID	2753450
InChI InChI=1S/C14H12Br2/c15-13(11-seven-three-1-four-viii-11)fourteen(16)12-9-five-ii-6-ten-12/h1-10,xiii-14H/t13-,fourteen+ Key: GKESIQQTGWVOLH-OKILXGFUSA-N
SMILES C1=CC=C(C=C1)[C@H]([C@H](C2=CC=CC=C2)Br)Br
Backdrop
Chemic formula	C 14 H 12 Br 2
Tooth mass	340.058 g·mol−1
Appearance	White solid
Melting betoken	241 °C (466 °F; 514 Yard)[two]
Dipole moment	0.four-0.9[1]
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Take chances statements	H302, H314
Precautionary statements	P260, P264, P270, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P332+P313, P337+P313, P362, P363, P405, P501
Except where otherwise noted, information are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Chemical chemical compound

meso-Stilbene dibromide is an organic compound with a formula of (C₆H_vCH(Br))₂.^[3]It is one of three isomeric stilbene dibromides, the others being the pair of enantiomers. All are white solids.^[four]

Synthesis and reactions [edit]

meso-Stilbene dibromide tin can be prepared past treatment of (Eastward)-stilbene with bromine.^[v]

Reaction of stilbene dibromide with base gives diphenylacetylene.^[4]

References [edit]

1. ^ Weissberger, A. (1945). "Dipole Moment and Structure of Organic Compounds. XVII.[1] The Electric Moments of α- and β-Stilbene Dibromide and of p-Diacetylbenzene". J. Am. Chem. Soc. 67 (v): 778–779. doi:ten.1021/ja01221a025.
2. ^ Kulangiappar, K.; Ramaprakash, M.; Vasudevan, D.; Raju, T. (2016). "Electrochemical bromination of cyclic and acyclic enes using biphase electrolysis". Constructed Communications. 46 (two): 145–153. doi:10.1080/00397911.2015.1125498. S2CID 101806740.
3. ^ Schroth, Werner; Zeitschrift für Chemie 1977, V17(ii), P56 CAPLUS
4. ^ ^{a b} Smith, Lee Irvin; Falkov, Yard. M. (1942). "Diphenylacetylene". Org. Synth. 22: 50. doi:10.15227/orgsyn.022.0050.
5. ^ Gilbert, J.C.; Martin, S.F. (2002). Experimental Organic Chemistry: A Miniscale and Macroscale Approach, third edition. London: Thomson. pp. 348–353. ISBN978-0-03-034048-2.

Meso Stilbene Dibromide Boiling Point,

Source: https://en.wikipedia.org/wiki/Meso-Stilbene_dibromide

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