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Home Deuterated Building Blocks 2901-80-6
2901-80-6,MFCD00038283
Catalog No.:AA002V4E

2901-80-6 | Benzoyl-dl-valine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
95%
in stock  
$13.00   $9.00
- +
100g
98%
in stock  
$112.00   $78.00
- +
500g
98%
in stock  
$494.00   $346.00
- +
  • 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:
AA002V4E
Chemical Name:
Benzoyl-dl-valine
CAS Number:
2901-80-6
Molecular Formula:
C12H15NO3
Molecular Weight:
221.2524
MDL Number:
MFCD00038283
SMILES:
CC([C@@H](C(=O)O)NC(=O)c1ccccc1)C
Properties
Properties
 
BP:
451.8°C at 760 mmHg  
Form:
Solid  
MP:
132°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
257  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
1  
XLogP3:
2.2  

Upstream Synthesis Route

[1]Patent:US5254548,1993,A,

[2]JournaloftheAmericanChemicalSociety,2014,vol.136,#51,p.17869-17881

[3]OrganicLetters,2018,vol.20,#22,p.7239-7244

[4]Patent:WO2012/69275,2012,A1,.Locationinpatent:Page/Pagecolumn118

[5]Patent:US2012/134934,2012,A1,.Locationinpatent:Page/Pagecolumn59-60

[6]EuropeanJournalofOrganicChemistry,2009,#3,p.378-386

[7]JournalofOrganicChemistry,2014,vol.79,#4,p.1542-1554

[8]JournalofBiologicalChemistry,1941,vol.138,p.627

[9]ChemischeBerichte,1902,vol.35,p.409

[10]RussianJournalofOrganicChemistry,1994,vol.30,#5.2,p.767-770

[11]ZhurnalOrganicheskoiKhimii,1994,vol.30,#5,p.723-725

[12]AustralianJournalofChemistry,1976,vol.29,p.339-356

[13]TetrahedronLetters,1986,vol.27,#14,p.1579-1582

[14]MonatsheftefurChemie,2000,vol.131,#6,p.667-672

[15]RevueRoumainedeChimie,1999,vol.44,#2,p.137-142

[16]JournalofOrganicChemistry,2002,vol.67,#18,p.6542-6545

[17]Patent:US5091378,1992,A,

[18]JournalofChemicalResearch,2011,vol.35,#8,p.468-470

[19]JournalofOrganicChemistry,2017,vol.82,#1,p.126-134

[1]JournalofOrganometallicChemistry,1991,vol.417,#1/2,p.253-276

[1]JournalofOrganicChemistry,1993,vol.58,#12,p.3252-3258

[2]JournalofOrganicChemistry,1993,vol.58,#12,p.3252-3258

[1]ChemischeBerichte,1902,vol.35,p.409

[1]RussianJournalofGeneralChemistry,2018,vol.88,#1,p.80-85

[2]Zh.Obshch.Khim.,2018,vol.88,#1,p.84-89,6

Downstream Synthesis Route

[1]ZhurnalObshcheiKhimii,1956,vol.26,p.2329,2334;engl.Ausg.S.2605,2609

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1958,vol.78,p.767    Chem.Abstr.,1958,p.18237

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1958,vol.78,p.767    Chem.Abstr.,1958,p.18237

[1]JournaloftheChemicalSociety,1957,p.2073,2077

[1]ArchivesofBiochemistry,1950,vol.25,p.21,26

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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