Catalog No.:AA00DU6Q

5453-98-5 | 2,3-Dihydro-1h-inden-5-ylacetic acid

Name: Name:2,3-Dihydro-1h-inden-5-ylacetic acid
Brand: AABLOCKS
SKU: AA00DU6Q
Availability: InStock
Rating: 90 (10 reviews)

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250mg

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$279.00 $195.00

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95%

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$620.00 $434.00

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

Technical Information

Catalog Number:

AA00DU6Q

Chemical Name:

2,3-Dihydro-1h-inden-5-ylacetic acid

CAS Number:

5453-98-5

Molecular Formula:

C11H12O2

Molecular Weight:

176.2118

MDL Number:

MFCD06378266

SMILES:

OC(=O)Cc1ccc2c(c1)CCC2

NSC Number:

18918

Properties

BP:

333°C at 760 mmHg

Form:

Solid

MP:

113-114℃

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

200

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

2.2

Downstream Synthesis Route

764-41-0

5453-98-5

854820-98-7

[1]CurrentPatentAssignee:NOVARTISAG;Novartis(w/oSandoz)-US2573015,1948,ACurrentPatentAssignee:NOVARTISAG;Novartis(w/oSandoz)-DE812669,1948,C[DRP/DRBPOrg.Chem.][DRP/DRBPOrg.Chem.]

5453-98-5

87073-79-8

[1]Fristad,WilliamE.;Klang,JeffreyA.[TetrahedronLetters,1983,vol.24,#22,p.2219-2222]

5453-98-5

125564-43-4

[1]Giardina;Clarke;Dondio;Petrone;Sbacchi;Vecchietti[JournalofMedicinalChemistry,1994,vol.37,#21,p.3482-3491]

158094-20-3

5453-98-5

[1]Giardina;Clarke;Dondio;Petrone;Sbacchi;Vecchietti[JournalofMedicinalChemistry,1994,vol.37,#21,p.3482-3491]

5453-98-5

((R)-5-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-methyl-amine;hydrochloride

2-Indan-5-yl-N-((R)-5-methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-N-methyl-acetamide

[1]Meyer,MichaelD.;Hancock,ArthurA.;Tietje,Karin;Sippy,KevinB.;Prasad,Rajnandan;Stout,DavidM.;Arendsen,DavidL.;Donner,B.Greg;Carroll,WilliamA.[JournalofMedicinalChemistry,1997,vol.40,#7,p.1049-1062]

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

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