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7569-62-2,MFCD02664695
Catalog No.:AA003BV4

7569-62-2 | (5-Chloro-2-methoxyphenyl)acetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$19.00   $14.00
- +
5g
98%
in stock  
$71.00   $50.00
- +
25g
98%
in stock  
$304.00   $213.00
- +
100g
98%
in stock  
$1,000.00   $700.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003BV4
Chemical Name:
(5-Chloro-2-methoxyphenyl)acetic acid
CAS Number:
7569-62-2
Molecular Formula:
C9H9ClO3
Molecular Weight:
200.6190
MDL Number:
MFCD02664695
SMILES:
COc1ccc(cc1CC(=O)O)Cl
Properties
Properties
 
BP:
323.5°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
184  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2  

Downstream Synthesis Route

[1]BulletindesSocietesChimiquesBelges,1980,vol.89,p.459-485

[2]BulletindelaSocieteChimiquedeFrance,1953,p.640,643

[3]BulletindelaSocieteChimiquedeFrance,1966,p.1335-1342

[4]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.3109-3112

[5]Patent:US2003/83335,2003,A1

[6]Patent:US2004/92529,2004,A1

[7]Patent:WO2004/9550,2004,A1.Locationinpatent:Page42;43

[1]Verhe;DeKimpe;DeBuyck;etal.[BulletindesSocietesChimiquesBelges,1980,vol.89,#6,p.459-485]

[2]Julia;Baillarge[BulletindelaSocieteChimiquedeFrance,1953,p.640,643]

[3]Brown,MatthewF.;Bahnck,KevinB.;Blumberg,LauraC.;Brissette,WilliamH.;Burrell,SaraA.;Driscoll,JamesP.;Fedeles,Flavia;Fisher,MichaelB.;Foti,RobertS.;Gladue,RonaldP.;Guzman-Martinez,Aikomari;Hayward,MatthewM.;Lira,PaulD.;Lillie,BrettM.;Lu,Yi;Lundquist,GregD.;McElroy,EricB.;McGlynn,MollyA.;Paradis,TimothyJ.;Poss,ChristopherS.;Roache,JamesH.;Shavnya,Andrei;Shepard,RichardM.;Trevena,KristenA.;Tylaska,LaurieA.[BioorganicandMedicinalChemistryLetters,2007,vol.17,#11,p.3109-3112]

[4]CurrentPatentAssignee:PFIZERINC-US2003/83335,2003,A1

[5]CurrentPatentAssignee:PFIZERINC-US2004/92529,2004,A1

[1]Julia,M.;Gaston-Breton,H.[BulletindelaSocieteChimiquedeFrance,1966,p.1335-1342]

[2]CurrentPatentAssignee:ALMIRALLSA-WO2006/133802,2006,A1Locationinpatent:Page/Pagecolumn66-67

[3]CurrentPatentAssignee:ENTERPRISETHERAPEUTICSLIMITED;ROCHEHOLDINGAG-WO2020/249956,2020,A1Locationinpatent:Page/Pagecolumn54

[1]Julia,M.;Gaston-Breton,H.[BulletindelaSocieteChimiquedeFrance,1966,p.1335-1342]

[1]Verhe;DeKimpe;DeBuyck;etal.[BulletindesSocietesChimiquesBelges,1980,vol.89,#6,p.459-485]

[2]Julia;Baillarge[BulletindelaSocieteChimiquedeFrance,1953,p.640,643]

[3]Munavalli,S.etal.[BulletindelaSocieteChimiquedeFrance,1966,p.3311-3318]

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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SDS
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