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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
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  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
8  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
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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Tags:33018-91-6 Molecular Formula|33018-91-6 MDL|33018-91-6 SMILES|33018-91-6 Ethyl hydrogen pimelate
Catalog No.: AA0034H5
33018-91-6,MFCD00014383
33018-91-6 | Ethyl hydrogen pimelate
Pack Size： 1g
Purity： 95%
in stock
$18.00 $13.00
Pack Size： 5g
Purity： 95%
in stock
$60.00 $42.00
Pack Size： 25g
Purity： 95%
in stock
$197.00 $138.00
Pack Size： 100g
Purity： 95%
in stock
$716.00 $502.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
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
BP: 135-138°C at 1 mmHg  
Form: Liquid  
MP: 10 °C  
Refractive Index: 1.442  
Storage: Keep in dry area;2-8℃;  
Complexity: 165  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 8  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.2  
Upstream Synthesis Route
2050-20-6    33018-91-6 

[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

111-16-0    2050-20-6    33018-91-6 

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

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

111-16-0    33018-91-6 

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

142-79-0    33018-91-6 

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

111-16-0    64-17-5    33018-91-6 

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

Downstream Synthesis Route
111-16-0    64-17-5    33018-91-6 

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

2050-20-6    33018-91-6 

[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

33018-91-6    6149-48-0 

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

188290-36-0    33018-91-6    122115-40-6 

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

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