Home Other Building Blocks 33018-91-6
33018-91-6,MFCD00014383
Catalog No.:AA0034H5

33018-91-6 | Ethyl hydrogen pimelate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$18.00   $13.00
- +
5g
95%
in stock  
$60.00   $42.00
- +
25g
95%
in stock  
$197.00   $138.00
- +
100g
95%
in stock  
$716.00   $502.00
- +
  • 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:
AA0034H5
Chemical Name:
Ethyl hydrogen pimelate
CAS Number:
33018-91-6
Molecular Formula:
C9H16O4
Molecular Weight:
188.2209
MDL Number:
MFCD00014383
SMILES:
CCOC(=O)CCCCCC(=O)O
Properties
Properties
 
BP:
135-138°C at 1 mmHg  
Form:
Liquid  
MP:
10 °C  
Refractive Index:
1.442  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
165  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
8  
XLogP3:
1.2  

Upstream Synthesis Route

[1]Patent:US2014/256775,2014,A1,.Locationinpatent:Paragraph0178;0183;0184

[2]JournalofMedicinalChemistry,2009,vol.52,#9,p.2776-2785

[3]BulletindelaSocieteChimiquedeFrance,1910,vol.<4>7,p.219

[4]JournaloftheChemicalSociety,1901,vol.79,p.1192

[5]BioorganicChemistry,1998,vol.26,#3,p.157-168

[6]Patent:WO2017/9651,2017,A1,.Locationinpatent:Page/Pagecolumn86;87

[1]JournaloftheAmericanChemicalSociety,1948,vol.70,p.304

[2]BulletindelaSocieteChimiquedeFrance,1929,vol.<4>45,p.841

[1]Patent:US2014/256775,2014,A1,

[1]Patent:US2014/256775,2014,A1,

[1]BulletindelaSocieteChimiquedeFrance,1910,vol.<4>7,p.219

Downstream Synthesis Route

[1]BulletindelaSocieteChimiquedeFrance,1910,vol.<4>7,p.219

[1]Patent:US2014/256775,2014,A1.Locationinpatent:Paragraph0178;0183;0184

[2]JournalofMedicinalChemistry,2009,vol.52,p.2776-2785

[3]Patent:US2019/241504,2019,A1.Locationinpatent:Paragraph0105;0108-0109

[4]BulletindelaSocieteChimiquedeFrance,1910,vol.<4>7,p.219

[5]JournaloftheChemicalSociety,1901,vol.79,p.1192

[6]BioorganicChemistry,1998,vol.26,p.157-168

[7]Patent:WO2017/9651,2017,A1.Locationinpatent:Page/Pagecolumn86;87

[1]BulletinoftheAcademyofSciencesoftheUSSRDivisionofChemicalScience,1965,p.348-349    IzvestiyaAkademiiNaukSSSR,SeriyaKhimicheskaya,1965,p.369-370

[1]JournalofMedicinalChemistry,1989,vol.32,p.2214-2221

Literature

Title: Khan S, et al. A selective BCL-XL PROTAC degrader achieves safe and potent antitumor activity. Nat Med. 2019 Dec;25(12):1938-1947.

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SDS
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