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137567-79-4 | 5-Cyclohexene-1,2,3,4-tetrol, (1R,2R,3R,4R)-
CAS No: 137567-79-4 Catalog No: AG0013KI MDL No:
Product Description
Catalog Number:
AG0013KI
Chemical Name:
5-Cyclohexene-1,2,3,4-tetrol, (1R,2R,3R,4R)-
CAS Number:
137567-79-4
Molecular Formula:
C6H10O4
Molecular Weight:
146.1412
IUPAC Name:
cyclohex-5-ene-1,2,3,4-tetrol
InChI:
InChI=1S/C6H10O4/c7-3-1-2-4(8)6(10)5(3)9/h1-10H
InChI Key:
LRUBQXAKGXQBHA-UHFFFAOYSA-N
SMILES:
O[C@@H]1[C@H](O)C=C[C@H]([C@H]1O)O
Properties
Complexity:
129
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
146.058g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
4
Isotope Atom Count:
0
Molecular Weight:
146.142g/mol
Monoisotopic Mass:
146.058g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
80.9A^2
Undefined Atom Stereocenter Count:
4
Undefined Bond Stereocenter Count:
0
XLogP3:
-2.1
Literature
| Title | Journal |
|---|---|
| Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds. | Steroids 20051215 |
| Synthesis, characterization and biological activity of oxovanadium (IV) complexes with cyclic polyalcohols. | Journal of inorganic biochemistry 20051201 |
| Diastereoselective synthesis of D- and L-myo-inositol 3,4,5,6-tetrakisphosphates from D-glucose via dihydroxylation of (+)-conduritol B derivatives. | Chemical & pharmaceutical bulletin 20040601 |
| Stereoselective synthesis of several azido/amino- and diazido/diamino-myo-inositols and their phosphates from p-benzoquinone. | Organic & biomolecular chemistry 20030607 |
| Common-intermediate strategy for synthesis of conduritols and inositols via beta-hydroxy cyclohexenylsilanes. | Organic letters 20030515 |
| Facile syntheses of all possible diastereomers of conduritol and various derivatives of inositol stereoisomers in high enantiopurity from myo-inositol. | The Journal of organic chemistry 20020517 |
| Efficient synthesis of enantiopure conduritols by ring-closing metathesis. | The Journal of organic chemistry 20010629 |
| Asymmetric induction of conduritols via AAA reactions: synthesis of the aminocyclohexitol of hygromycin A. | Chemistry (Weinheim an der Bergstrasse, Germany) 20010417 |
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