Catalog No.:AA003JEI

456-47-3 | 3-Fluorobenzyl alcohol

Name: Name:3-Fluorobenzyl alcohol
Brand: AABLOCKS
SKU: AA003JEI
Availability: InStock
Rating: 90 (10 reviews)

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96%

in stock

$7.00 $5.00

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10g

96%

in stock

$9.00 $7.00

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25g

96%

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$21.00 $15.00

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100g

96%

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003JEI

Chemical Name:

3-Fluorobenzyl alcohol

CAS Number:

456-47-3

Molecular Formula:

C7H7FO

Molecular Weight:

126.1283

MDL Number:

MFCD00004631

SMILES:

OCc1cccc(c1)F

NSC Number:

158273

Properties

BP:

204.5°C at 760 mmHg

Form:

Liquid

Refractive Index:

n20/D 1.513(lit.)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

1.5

Upstream Synthesis Route

456-47-3

456-41-7

[1]NipponKagakuZasshi,1958,vol.79,p.1428,1430

[2]Chem.Abstr.,1960,p.5518

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[4]EuropeanJournalofMedicinalChemistry,2017,vol.127,p.100-114

456-47-3

456-42-8

[1]JournaloftheChemicalSociety,1935,p.1815,1818

456-48-4

100-82-3

456-47-3

[1]OrganicLetters,2002,vol.4,#12,p.2055-2058

455-68-5

391-92-4

392-04-1

456-47-3

[1]OrganicandBiomolecularChemistry,2008,vol.6,#7,p.1251-1259

455-68-5

391-92-4

392-04-1

456-47-3

[1]OrganicandBiomolecularChemistry,2008,vol.6,#7,p.1251-1259

Downstream Synthesis Route

456-47-3

456-48-4

[1]ChemischeBerichte,1990,vol.123,p.1357-1364

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102606-95-1

456-47-3

[1]Wan,Peter;Chak,Becky;Li,Carrier[TetrahedronLetters,1986,vol.27,#26,p.2937-2940]

456-47-3

75-36-5

102606-95-1

[1]Wan,Peter;Chak,Becky;Li,Carrier[TetrahedronLetters,1986,vol.27,#26,p.2937-2940]

456-47-3

39416-48-3

C7H7FO*C5H5N*Br3H

[1]JournalofChemicalResearch,Miniprint,1995,p.1734-1758

C7H7FO*C5H5N*Br3H

456-47-3

39416-48-3

[1]JournalofChemicalResearch,Miniprint,1995,p.1734-1758

Literature

Title: Primary amino acid derivatives: substitution of the 4'-N'-benzylamide site in (R)-N'-benzyl 2-amino-3-methylbutanamide, (R)-N'-benzyl 2-amino-3,3-dimethylbutanamide, and (R)-N'-benzyl 2-amino-3-methoxypropionamide provides potent anticonvulsants with pain-attenuating properties.

Journal: Journal of medicinal chemistry 20111013

Title: Two polymorphs of safinamide, a selective and reversible inhibitor of monoamine oxidase B.

Journal: Acta crystallographica. Section C, Crystal structure communications 20100601

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