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Details

Stereochemistry RACEMIC
Molecular Formula C16H24N2O4
Molecular Weight 308.3728
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of tert-Butyl (1-(benzylamino)-3-methoxy-1-oxopropan-2-yl)carbamate

SMILES

COCC(NC(=O)OC(C)(C)C)C(=O)NCC1=CC=CC=C1

InChI

InChIKey=ZEWWJSJMNBJIKR-UHFFFAOYSA-N
InChI=1S/C16H24N2O4/c1-16(2,3)22-15(20)18-13(11-21-4)14(19)17-10-12-8-6-5-7-9-12/h5-9,13H,10-11H2,1-4H3,(H,17,19)(H,18,20)

HIDE SMILES / InChI

Molecular Formula C16H24N2O4
Molecular Weight 308.3728
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 19:17:18 GMT 2025
Edited
by admin
on Wed Apr 02 19:17:18 GMT 2025
Record UNII
MUR75W8MCL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(1-Benzylcarbamoyl-2-methoxy-ethyl)-carbamic acid tert-butyl ester
Preferred Name English
tert-Butyl (1-(benzylamino)-3-methoxy-1-oxopropan-2-yl)carbamate
Systematic Name English
1,1-Dimethylethyl N-[1-(methoxymethyl)-2-oxo-2-[(phenylmethyl)amino]ethyl]carbamate
Systematic Name English
tert-Butyl N-[2-(benzylamino)-1-(methoxymethyl)-2-oxo-ethyl]carbamate
Systematic Name English
Carbamic acid, N-[1-(methoxymethyl)-2-oxo-2-[(phenylmethyl)amino]ethyl]-, 1,1-dimethylethyl ester
Systematic Name English
2-Methyl-2-propanyl [1-(benzylamino)-3-methoxy-1-oxo-2-propanyl]carbamate
Systematic Name English
Code System Code Type Description
FDA UNII
MUR75W8MCL
Created by admin on Wed Apr 02 19:17:18 GMT 2025 , Edited by admin on Wed Apr 02 19:17:18 GMT 2025
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CAS
1352305-14-6
Created by admin on Wed Apr 02 19:17:18 GMT 2025 , Edited by admin on Wed Apr 02 19:17:18 GMT 2025
PRIMARY
PUBCHEM
23116001
Created by admin on Wed Apr 02 19:17:18 GMT 2025 , Edited by admin on Wed Apr 02 19:17:18 GMT 2025
PRIMARY
EPA CompTox
DTXSID80630748
Created by admin on Wed Apr 02 19:17:18 GMT 2025 , Edited by admin on Wed Apr 02 19:17:18 GMT 2025
PRIMARY