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Details

Stereochemistry ABSOLUTE
Molecular Formula C38H32N2O5
Molecular Weight 596.6711
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-(tritylamino)butanoic acid, (2R)-

SMILES

OC(=O)[C@@H](CC(=O)NC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46

InChI

InChIKey=KJYAFJQCGPUXJY-UUWRZZSWSA-N
InChI=1S/C38H32N2O5/c41-35(40-38(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28)24-34(36(42)43)39-37(44)45-25-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33/h1-23,33-34H,24-25H2,(H,39,44)(H,40,41)(H,42,43)/t34-/m1/s1

HIDE SMILES / InChI

Molecular Formula C38H32N2O5
Molecular Weight 596.6711
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 19:54:52 GMT 2023
Edited
by admin
on Sat Dec 16 19:54:52 GMT 2023
Record UNII
9M9EUZ5N47
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-(tritylamino)butanoic acid, (2R)-
Common Name English
(R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-(tritylamino)butanoic acid
Common Name English
N<SUP>2</SUP>-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-(triphenylmethyl)-D-asparagine
Common Name English
D-Asparagine, N<SUP>2</SUP>-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(triphenylmethyl)-
Common Name English
Fmoc-D-Asn(Trt)-OH
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID10647445
Created by admin on Sat Dec 16 19:54:52 GMT 2023 , Edited by admin on Sat Dec 16 19:54:52 GMT 2023
PRIMARY
CAS
180570-71-2
Created by admin on Sat Dec 16 19:54:52 GMT 2023 , Edited by admin on Sat Dec 16 19:54:52 GMT 2023
PRIMARY
PUBCHEM
24820182
Created by admin on Sat Dec 16 19:54:52 GMT 2023 , Edited by admin on Sat Dec 16 19:54:52 GMT 2023
PRIMARY
FDA UNII
9M9EUZ5N47
Created by admin on Sat Dec 16 19:54:52 GMT 2023 , Edited by admin on Sat Dec 16 19:54:52 GMT 2023
PRIMARY
Related Record Type Details
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