Home Other Building Blocks D-(+)-Malic acid

D-(+)-Malic acid

CAS No.:
636-61-3
Catalog Number:
AG0032FC
Molecular Formula:
C4H6O5
Molecular Weight:
134.0874
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$19
- +
25g
≥98%
In Stock USA
United States
$46
- +
100g
98%
In Stock USA
United States
$138
- +
500g
98%
In Stock USA
United States
$563
- +
Product Description
Catalog Number:
AG0032FC
Chemical Name:
D-(+)-Malic acid
CAS Number:
636-61-3
Molecular Formula:
C4H6O5
Molecular Weight:
134.0874
MDL Number:
MFCD00004245
IUPAC Name:
(2R)-2-hydroxybutanedioic acid
InChI:
InChI=1S/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9)/t2-/m1/s1
InChI Key:
BJEPYKJPYRNKOW-UWTATZPHSA-N
SMILES:
OC(=O)C[C@H](C(=O)O)O
EC Number:
211-262-2
UNII:
P750Y95K96
Properties
Complexity:
129  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
134.022g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
134.087g/mol
Monoisotopic Mass:
134.022g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
94.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.3  
Literature
Title Journal
AcsD catalyzes enantioselective citrate desymmetrization in siderophore biosynthesis. Nature chemical biology 20090301
Total synthesis of leustroducsin B. The Journal of organic chemistry 20080718
Substrate specificity analysis and inhibitor design of homoisocitrate dehydrogenase. Bioorganic & medicinal chemistry 20070201
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Diversity of function in the isocitrate lyase enzyme superfamily: the Dianthus caryophyllus petal death protein cleaves alpha-keto and alpha-hydroxycarboxylic acids. Biochemistry 20051220
A total synthesis of hydroxylysine in protected form and investigations of the reductive opening of p-methoxybenzylidene acetals. The Journal of organic chemistry 20041210
Total synthesis of an antitumor antibiotic, Fostriecin (CI-920). Journal of the American Chemical Society 20030709
Total synthesis and structure confirmation of the annonaceous acetogenins 30(S)-hydroxybullatacin, uvarigrandin a, and 5(R)-uvarigrandin a (narumicin I?). The Journal of organic chemistry 20030307
Properties