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4835-90-9,MFCD00059953
Catalog No.:AA003JI4

4835-90-9 | 2,2-Dimethyl-3-hydroxypropionic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
97%
in stock  
$6.00   $4.00
- +
25g
97%
in stock  
$13.00   $9.00
- +
100g
97%
in stock  
$43.00   $30.00
- +
500g
95%
in stock  
$127.00   $89.00
- +
  • 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:
AA003JI4
Chemical Name:
2,2-Dimethyl-3-hydroxypropionic acid
CAS Number:
4835-90-9
Molecular Formula:
C5H10O3
Molecular Weight:
118.1311
MDL Number:
MFCD00059953
SMILES:
OCC(C(=O)O)(C)C
NSC Number:
115936
Properties
Properties
 
BP:
242.8°C at 760 mmHg  
Form:
Liquid  
MP:
−16 °C(lit.)  
Refractive Index:
n20/D 1.5215(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
95.8  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  

Upstream Synthesis Route

[1]Patent:WO2012/10651,2012,A2,

[1]Patent:WO2014/145023,2014,A1,.Locationinpatent:Paragraph0390

[2]BulletindelaSocieteChimiquedeFrance,1904,vol.<3>31,p.129

[1]Patent:US5877317,1999,A,

[1]CatalysisLetters,2012,vol.142,#9,p.1114-1120

[2]Chemistry-AEuropeanJournal,2013,vol.19,#35,p.11725-11732

[1]CatalysisLetters,2012,vol.142,#9,p.1114-1120

Downstream Synthesis Route

[1]BulletindelaSocieteChimiquedeFrance,1904,vol.<3>31,p.129

[2]JournalofOrganicChemistry,1973,vol.38,p.2346-2350

[3]JournaloftheAmericanChemicalSociety,1962,vol.84,p.3307-3319

[1]MonatsheftefurChemie,1906,vol.27,p.955

[1]Patent:WO2012/10651,2012,A2.Locationinpatent:Page/Pagecolumn20

[2]BulletindelaSocieteChimiquedeFrance,1904,vol.<3>31,p.155

[3]MonatsheftefurChemie,1907,vol.28,p.1056

[4]ChemischeBerichte,1959,vol.92,p.1329,1334

[5]MonatsheftefurChemie,1907,vol.28,p.1056

[6]CanadianJournalofChemistry,1971,vol.49,p.3866-3876

[7]Patent:US5998400,1999,A

[8]Patent:US4405357,1983,A

[9]Patent:WO2019/118612,2019,A1.Locationinpatent:Paragraph0252

[1]BioorganicandMedicinalChemistry,2007,vol.15,p.3896-3911

[2]Patent:WO2019/126731,2019,A1.Locationinpatent:Paragraph0627

[3]Patent:WO2008/7930,2008,A1.Locationinpatent:Page/Pagecolumn29

[4]Patent:US2010/120783,2010,A1.Locationinpatent:Page/Pagecolumn11

[5]Patent:WO2010/56022,2010,A2.Locationinpatent:Page/Pagecolumn24-25

[6]Patent:WO2011/73172,2011,A1.Locationinpatent:Page/Pagecolumn47-48

[7]Patent:US2011/152257,2011,A1.Locationinpatent:Page/Pagecolumn35

[8]Patent:WO2014/64134,2014,A1.Locationinpatent:Page/Pagecolumn89

[9]BulletindelaSocieteChimiquedeFrance,1904,vol.<3>31,p.129

[10]Patent:US4665091,1987,A

[11]Patent:US4668699,1987,A

[12]Patent:EP211416,1991,B1

[13]Chemistry-AEuropeanJournal,2014,vol.20,p.9530-9533

[1]JournaloftheAmericanChemicalSociety,1980,vol.102,p.7026-7032

[2]ChemischeBerichte,1973,vol.106,p.2246-2254

Literature

Title: Joint experimental and theoretical studies of the mechanism for the gas phase elimination kinetics of methyl 2,2-dimethyl-3-hydroxypropionate.

Journal: The journal of physical chemistry. A 20090416

Title: A concise method for the preparation of peptide and arginine-rich peptide-conjugated antisense oligonucleotide.

Journal: Bioconjugate chemistry 20030101

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SDS
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