ChemicalBook--->CAS DataBase List--->4549-33-1

4549-33-1

4549-33-1 Structure

4549-33-1 Structure
IdentificationMore
[Name]

1,9-DIBROMONONANE
[CAS]

4549-33-1
[Synonyms]

1,9-DIBROMONONANE
NONAMETHYLENE BROMIDE
NONAMETHYLENE DIBROMIDE
1,9-Dibromnonan
1,9-dibromo-nonan
Nonane,1,9-dibromo-
1 9-DIBROMONONANE 97% (GC)
1,9-Dibromononane,97%
Nonamethylendibromid
1,9-Nonanediyl dibromide
[EINECS(EC#)]

224-913-0
[Molecular Formula]

C9H18Br2
[MDL Number]

MFCD00000279
[Molecular Weight]

286.05
[MOL File]

4549-33-1.mol
Chemical PropertiesBack Directory
[Appearance]

CLEAR COLOURLESS TO SLIGHTLY YELLOW LIQUID
[Melting point ]

-2 °C
[Boiling point ]

285-288 °C (lit.)
[density ]

1.407 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.496(lit.)
[Fp ]

>230 °F
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Liquid
[color ]

Clear colorless to yellow
[BRN ]

1737598
[InChI]

InChI=1S/C9H18Br2/c10-8-6-4-2-1-3-5-7-9-11/h1-9H2
[InChIKey]

WGAXVZXBFBHLMC-UHFFFAOYSA-N
[SMILES]

C(Br)CCCCCCCCBr
[CAS DataBase Reference]

4549-33-1(CAS DataBase Reference)
[EPA Substance Registry System]

Nonane, 1,9-dibromo- (4549-33-1)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[TSCA ]

Yes
[HS Code ]

29033990
[Storage Class]

10 - Combustible liquids
Hazard InformationBack Directory
[Chemical Properties]

CLEAR COLOURLESS TO SLIGHTLY YELLOW LIQUID
[Uses]

1,9-Dibromononane is a useful research chemical compound.
[Synthesis]

1,9-Nonanediol

3937-56-2

1,9-DIBROMONONANE

4549-33-1

General procedure: In a dry reaction flask equipped with a stir bar, copper catalyst (2 mg, 0.002 mmol, 0.01 eq.), 1,9-nonanediol (0.20 mmol, 1.0 eq.), carbon tetrabromide (131.6 mg, 0.4 mmol, 2.0 eq.), and sodium bromide (41 mg, 0.40 mmol, 2.0 eq.) were added in sequence. The reaction vial was sealed and after displacing the air with nitrogen, anhydrous DMF (1.5 mL) was added via syringe. The reaction mixture was stirred under the light of a purple LED (394 nm) for 24 hours. Upon completion of the reaction, the mixture was transferred to a partitioning funnel and layered with ether (10 mL) and water (10 mL). The aqueous layer was separated and extracted with ether (2 x 10 mL). The organic layers were combined and washed sequentially with saturated aqueous NaHCO3 solution, Na2S2O3 solution and brine, dried with anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (100% hexane as eluent) to afford the target product 1,9-dibromononane.

[References]

[1] Beilstein Journal of Organic Chemistry, 2018, vol. 14, p. 2730 - 2736
[2] Nippon Kagaku Zasshi, 1957, vol. 78, p. 1504
[3] Chem.Abstr., 1960, p. 1540
[4] Bulletin de la Societe Chimique de France, 1957, p. 1463,1467
[5] Biochemical Journal, 1947, vol. 41, p. 57
Spectrum DetailBack Directory
[Spectrum Detail]

1,9-DIBROMONONANE(4549-33-1)MS
1,9-DIBROMONONANE(4549-33-1)1HNMR
1,9-DIBROMONONANE(4549-33-1)13CNMR
1,9-DIBROMONONANE(4549-33-1)IR1
1,9-DIBROMONONANE(4549-33-1)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

1,9-Dibromononane, 97%(4549-33-1)
[Alfa Aesar]

1,9-Dibromononane, 97%(4549-33-1)
[Sigma Aldrich]

4549-33-1(sigmaaldrich)
[TCI AMERICA]

1,9-Dibromononane,>95.0%(GC)(4549-33-1)
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