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Details

Stereochemistry ACHIRAL
Molecular Formula C5H11NO
Molecular Weight 101.1469
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-TERT-BUTYLFORMAMIDE

SMILES

CC(C)(C)NC=O

InChI

InChIKey=SDLAKRCBYGZJRW-UHFFFAOYSA-N
InChI=1S/C5H11NO/c1-5(2,3)6-4-7/h4H,1-3H3,(H,6,7)

HIDE SMILES / InChI

Molecular Formula C5H11NO
Molecular Weight 101.1469
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Induction of cytotoxicity, apoptosis and cell cycle arrest by 1-t-butyl carbamoyl, 7-methyl-indole-3-ethyl isothiocyanate (NB7M) in nervous system cancer cells.
2009-02-06
Di-tert-butyl N,N'-(octa-hydro-penta-lene-2,5-di-yl)dicarbamate.
2008-05-24
Solvation properties of N-substituted cis and trans amides are not identical: significant enthalpy and entropy changes are revealed by the use of variable temperature 1H NMR in aqueous and chloroform solutions and ab initio calculations.
2005-12-29
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:22:51 GMT 2025
Edited
by admin
on Mon Mar 31 22:22:51 GMT 2025
Record UNII
GZ0P5X0IRF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-TERT-BUTYLFORMAMIDE
Systematic Name English
NSC-7082
Preferred Name English
N-(1,1-DIMETHYLETHYL)FORMAMIDE
Systematic Name English
N-FORMYL-TERT-BUTYLAMINE
Systematic Name English
N-T-BUTYLFORMAMIDE [HSDB]
Common Name English
FORMAMIDE, N-(TERT-BUTYL)-
Systematic Name English
TERT-BUTYLFORMAMIDE
Systematic Name English
FORMAMIDE, N-(1,1-DIMETHYLETHYL)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID2062408
Created by admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
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NSC
7082
Created by admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
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PUBCHEM
17045
Created by admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
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FDA UNII
GZ0P5X0IRF
Created by admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
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CAS
2425-74-3
Created by admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
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HSDB
5877
Created by admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
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ECHA (EC/EINECS)
219-369-6
Created by admin on Mon Mar 31 22:22:51 GMT 2025 , Edited by admin on Mon Mar 31 22:22:51 GMT 2025
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