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Details

Stereochemistry EPIMERIC
Molecular Formula C30H54O4Si2
Molecular Weight 534.9184
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-(tert-butyldimethylsilyloxy)-4-((R)-3-(tert-butyldimethylsilyloxy)-5-phenylpentyl)hexahydro-2H-cyclopenta[b]furan-2-ol, (3aR,4R,5R,6aS)-

SMILES

CC(C)(C)[Si](C)(C)O[C@H](CC[C@H]1[C@@H](C[C@@H]2OC(O)C[C@H]12)O[Si](C)(C)C(C)(C)C)CCC3=CC=CC=C3

InChI

InChIKey=ARZBNFLNPFDIAZ-YSWLZDFMSA-N
InChI=1S/C30H54O4Si2/c1-29(2,3)35(7,8)33-23(17-16-22-14-12-11-13-15-22)18-19-24-25-20-28(31)32-26(25)21-27(24)34-36(9,10)30(4,5)6/h11-15,23-28,31H,16-21H2,1-10H3/t23-,24+,25+,26-,27+,28?/m0/s1

HIDE SMILES / InChI

Molecular Formula C30H54O4Si2
Molecular Weight 534.9184
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 5 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 18:18:44 GMT 2025
Edited
by admin
on Wed Apr 02 18:18:44 GMT 2025
Record UNII
L39E26L4V3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-(tert-butyldimethylsilyloxy)-4-((R)-3-(tert-butyldimethylsilyloxy)-5-phenylpentyl)hexahydro-2H-cyclopenta[b]furan-2-ol, (3aR,4R,5R,6aS)-
Systematic Name English
(3aR,4R,5R,6aS)-5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-[(3R)-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-5-phenylpentyl]hexahydro-2H-cyclopenta[b]furan-2-ol
Preferred Name English
2H-Cyclopenta[b]furan-2-ol, 5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[(3R)-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-5-phenylpentyl]hexahydro-, (3aR,4R,5R,6aS)-
Systematic Name English
Code System Code Type Description
PUBCHEM
70945646
Created by admin on Wed Apr 02 18:18:44 GMT 2025 , Edited by admin on Wed Apr 02 18:18:44 GMT 2025
PRIMARY
CAS
1240483-22-0
Created by admin on Wed Apr 02 18:18:44 GMT 2025 , Edited by admin on Wed Apr 02 18:18:44 GMT 2025
PRIMARY
FDA UNII
L39E26L4V3
Created by admin on Wed Apr 02 18:18:44 GMT 2025 , Edited by admin on Wed Apr 02 18:18:44 GMT 2025
PRIMARY