Home Bromides 201940-08-1
201940-08-1,MFCD09953049
Catalog No.:AA0027U4

201940-08-1 | tert-Butyl 5-bromoisoindoline-2-carboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$9.00   $7.00
- +
1g
95%
in stock  
$22.00   $15.00
- +
5g
95%
in stock  
$47.00   $33.00
- +
10g
95%
in stock  
$91.00   $64.00
- +
25g
95%
in stock  
$225.00   $158.00
- +
100g
95%
in stock  
$899.00   $630.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0027U4
Chemical Name:
tert-Butyl 5-bromoisoindoline-2-carboxylate
CAS Number:
201940-08-1
Molecular Formula:
C13H16BrNO2
Molecular Weight:
298.1756
MDL Number:
MFCD09953049
SMILES:
Brc1ccc2c(c1)CN(C2)C(=O)OC(C)(C)C
Properties
Properties
 
BP:
354.7°C at 760 mmHg  
Form:
Solid  
MP:
54-56°C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
300  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
2.9  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2016,vol.138,#41,p.13493-13496

[2]AngewandteChemie-InternationalEdition,2018,vol.57,#7,p.1968-1972

[3]Angew.Chem.,2018,vol.130,p.1986-1990,5

[1]Patent:US2017/275301,2017,A1,.Locationinpatent:Paragraph0226;0228

[2]Patent:EP3257857,2017,A1,.Locationinpatent:Paragraph0102;0104

[3]JournalofOrganicChemistry,2012,vol.77,#24,p.11296-11301

[4]Patent:WO2015/54317,2015,A1,.Locationinpatent:Paragraph0272;0273

[5]Patent:EP2311810,2011,A1,.Locationinpatent:Page/Pagecolumn24

[6]Patent:WO2014/89324,2014,A1,.Locationinpatent:Paragraph0236

[7]Patent:CN104016979,2017,B,.Locationinpatent:Paragraph0602;0603;0604;0605

[8]Patent:WO2008/76954,2008,A2,.Locationinpatent:Page/Pagecolumn54

[9]JournalofMedicinalChemistry,2007,vol.50,#2,p.199-210

[10]Patent:US2008/171754,2008,A1,.Locationinpatent:Page/Pagecolumn103

[11]Patent:WO2008/44029,2008,A1,.Locationinpatent:Page/Pagecolumn235

[12]Patent:WO2008/44041,2008,A1,.Locationinpatent:Page/Pagecolumn257

[13]Patent:WO2008/44045,2008,A1,.Locationinpatent:Page/Pagecolumn310

[14]Patent:WO2008/44054,2008,A2,.Locationinpatent:Page/Pagecolumn154

[15]BioorganicandMedicinalChemistryLetters,2008,vol.18,#14,p.4159-4162

[16]Patent:US2010/152184,2010,A1,.Locationinpatent:Page/Pagecolumn97

[17]JournalofMedicinalChemistry,2010,vol.53,#16,p.5956-5969

[18]BioorganicandMedicinalChemistryLetters,2011,vol.21,#16,p.4909-4912

[1]Patent:WO2017/40449,2017,A1,.Locationinpatent:Paragraph00449

[1]Patent:EP3192791,2017,A1,.Locationinpatent:Paragraph0599

[2]BioorganicandMedicinalChemistryLetters,2018,vol.28,#18,p.3050-3056

[1]JournalofMedicinalChemistry,2007,vol.50,#2,p.199-210

[2]BioorganicandMedicinalChemistryLetters,2011,vol.21,#16,p.4909-4912

[3]JournalofOrganicChemistry,2012,vol.77,#24,p.11296-11301

[4]Patent:WO2014/89324,2014,A1,

[5]Patent:WO2015/54317,2015,A1,

[6]Patent:CN104016979,2017,B,

[7]Patent:US2017/275301,2017,A1,

[8]Patent:EP3257857,2017,A1,

Downstream Synthesis Route

[1]Patent:US2017/275301,2017,A1.Locationinpatent:Paragraph0226;0228

[2]Patent:EP3257857,2017,A1.Locationinpatent:Paragraph0102;0104

[3]JournalofOrganicChemistry,2012,vol.77,p.11296-11301

[4]Patent:WO2015/54317,2015,A1.Locationinpatent:Paragraph0272;0273

[5]Patent:CN110294744,2019,A.Locationinpatent:Paragraph0163-0165;0189-0191

[6]Patent:EP2311810,2011,A1.Locationinpatent:Page/Pagecolumn24

[7]Patent:WO2014/89324,2014,A1.Locationinpatent:Paragraph0236

[8]Patent:CN104016979,2017,B.Locationinpatent:Paragraph0602;0603;0604;0605

[9]Patent:US2019/375744,2019,A1.Locationinpatent:Paragraph0107;0109

[10]JournalofMedicinalChemistry,2019,vol.62,p.7431-7444

[11]Patent:WO2008/76954,2008,A2.Locationinpatent:Page/Pagecolumn54

[12]JournalofMedicinalChemistry,2007,vol.50,p.199-210

[13]Patent:US2008/171754,2008,A1.Locationinpatent:Page/Pagecolumn103

[14]Patent:WO2008/44029,2008,A1.Locationinpatent:Page/Pagecolumn235

[15]Patent:WO2008/44041,2008,A1.Locationinpatent:Page/Pagecolumn257

[16]Patent:WO2008/44045,2008,A1.Locationinpatent:Page/Pagecolumn310

[17]Patent:WO2008/44054,2008,A2.Locationinpatent:Page/Pagecolumn154

[18]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.4159-4162

[19]Patent:US2010/152184,2010,A1.Locationinpatent:Page/Pagecolumn97

[20]JournalofMedicinalChemistry,2010,vol.53,p.5956-5969

[21]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.4909-4912

[1]Patent:WO2019/244049,2019,A1.Locationinpatent:Paragraph00180;00212;00214

[2]JournalofMedicinalChemistry,2007,vol.50,p.199-210

[3]Patent:WO2014/89324,2014,A1.Locationinpatent:Paragraph0237

[4]Patent:CN104016979,2017,B.Locationinpatent:Paragraph0606;0607;0608;0609

[5]Patent:US2008/171754,2008,A1.Locationinpatent:Page/Pagecolumn103

[6]Patent:US2019/192668,2019,A1.Locationinpatent:Paragraph2685;2686

[7]Patent:WO2010/10186,2010,A1.Locationinpatent:Page/Pagecolumn58

[8]Patent:WO2010/145202,2010,A1.Locationinpatent:Page/Pagecolumn59

[9]Patent:WO2015/112441,2015,A1.Locationinpatent:Page/Pagecolumn56

[10]Patent:US2016/333021,2016,A1.Locationinpatent:Paragraph0345

[1]Patent:US2005/267018,2005,A1

201940-08-1   
9-cyclopropyl-7-(2,3-dihydro-1H-isoindol-5-yl)-8-methoxy-9H-isothiazolo5,4-bquinoline-3,4-dione 

[1]JournalofMedicinalChemistry,2007,vol.50,p.199-210

201940-08-1   
9-cyclopropyl-7-(2,3-dihydro-1H-isoindol-5-yl)-6-fiuoro-9H-isothiazolo5,4-bquinoline-3,4-dione 

[1]JournalofMedicinalChemistry,2007,vol.50,p.199-210

Literature
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Tags:201940-08-1 Molecular Formula|201940-08-1 MDL|201940-08-1 SMILES|201940-08-1 tert-Butyl 5-bromoisoindoline-2-carboxylate