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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H15NO5
Molecular Weight 205.2084
Optical Activity ( - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-tert-Butoxycarbonyl-D-serine

SMILES

CC(C)(C)OC(=O)N[C@H](CO)C(O)=O

InChI

InChIKey=FHOAKXBXYSJBGX-RXMQYKEDSA-N
InChI=1S/C8H15NO5/c1-8(2,3)14-7(13)9-5(4-10)6(11)12/h5,10H,4H2,1-3H3,(H,9,13)(H,11,12)/t5-/m1/s1

HIDE SMILES / InChI

Molecular Formula C8H15NO5
Molecular Weight 205.2084
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 Mon Mar 31 23:43:45 GMT 2025
Edited
by admin
on Mon Mar 31 23:43:45 GMT 2025
Record UNII
B7N4S576WF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EC 444-670-6
Preferred Name English
N-tert-Butoxycarbonyl-D-serine
Systematic Name English
BOC-D-Serine
Common Name English
(R)-tert-Butoxycarbonyl-D-serine
Common Name English
(2R)-2-[[(tert-Butoxy)carbonyl]amino]-3-hydroxypropanoic acid
Systematic Name English
(R)-2-(tert-Butoxycarbonylamino)-3-hydroxypropanoic acid
Systematic Name English
N-[(1,1-Dimethylethoxy)carbonyl]-D-serine
Systematic Name English
D-Serine, N-[(1,1-dimethylethoxy)carbonyl]-
Systematic Name English
N-Boc-D-serine
Common Name English
(2R)-3-Hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Systematic Name English
tert-(Butoxycarbonyl)-D-serine
Systematic Name English
Code System Code Type Description
FDA UNII
B7N4S576WF
Created by admin on Mon Mar 31 23:43:45 GMT 2025 , Edited by admin on Mon Mar 31 23:43:45 GMT 2025
PRIMARY
PUBCHEM
7036280
Created by admin on Mon Mar 31 23:43:45 GMT 2025 , Edited by admin on Mon Mar 31 23:43:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID10348465
Created by admin on Mon Mar 31 23:43:45 GMT 2025 , Edited by admin on Mon Mar 31 23:43:45 GMT 2025
PRIMARY
CAS
6368-20-3
Created by admin on Mon Mar 31 23:43:45 GMT 2025 , Edited by admin on Mon Mar 31 23:43:45 GMT 2025
PRIMARY
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