Chemistry, asked by nivedithachiru, 3 months ago

Anisole structure.Spammed answers reported.​

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Answered by logitharun
0

Answer:

Anisole, or methoxybenzene, is an organic compound with the formula CH3OC6H5. It is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances. The compound is mainly made synthetically and is a precursor to other synthetic compounds. It is an ether.

Answered by shreyash7121
2

Anisole, or methoxybenzene, is an organic compound with the formula CH3OC6H5. It is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances. The compound is mainly made synthetically and is a precursor to other synthetic compounds. It is an ether.

Anisole

Anisol.svg

Anisole-3D-balls.png

Anisole.jpg

Names

Preferred IUPAC name

Anisole[1]

Systematic IUPAC name

Methoxybenzene[1]

Other names

Methyl phenyl ether[1]

Phenoxymethane

Identifiers

CAS Number

100-66-3 check

3D model (JSmol)

Interactive image

Beilstein Reference

506892

ChEBI

CHEBI:16579 check

ChEMBL

ChEMBL278024 check

ChemSpider

7238 check

ECHA InfoCard

100.002.615 Edit this at Wikidata

EC Number

202-876-1

Gmelin Reference

2964

KEGG

C01403 check

PubChem CID

7519

RTECS number

BZ8050000

UNII

B3W693GAZH check

UN number

2222

Properties

Chemical formula

C7H8O

Molar mass

108.140 g·mol−1

Appearance

Colorless liquid

Density

0.995 g/cm3

Melting point

−37 °C (−35 °F; 236 K)

Boiling point

154 °C (309 °F; 427 K)

Solubility

Insoluble

Magnetic susceptibility (χ)

-72.79·10−6 cm3/mol

Hazards

GHS pictograms

GHS02: FlammableGHS07: Harmful

GHS Signal word

Warning

GHS hazard statements

H226, H315, H319

GHS precautionary statements

P210, P233, P240, P241, P242, P243, P264, P280, P302+352, P303+361+353, P305+351+338, P321, P332+313, P337+313, P362, P370+378, P403+235, P501

NFPA 704 (fire diamond)

NFPA 704 four-colored diamond

220

Lethal dose or concentration (LD, LC):

LD50 (median dose)

3700 mg/kg (rat, oral)

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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Infobox references

It can be prepared by the Williamson ether synthesis; sodium phenoxide is reacted with a methyl halide to yield anisole.

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