Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H24N2 |
Molecular Weight | 172.311 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)NCCNC(C)(C)C
InChI
InChIKey=KGHYGBGIWLNFAV-UHFFFAOYSA-N
InChI=1S/C10H24N2/c1-9(2,3)11-7-8-12-10(4,5)6/h11-12H,7-8H2,1-6H3
Molecular Formula | C10H24N2 |
Molecular Weight | 172.311 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Structure-activity studies leading to ethambutol, a new type of antituberculous compound. | 1966 Apr 20 |
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A stabilized mu-eta(2):eta(2) peroxodicopper(II) complex with a secondary diamine ligand and its tyrosinase-like reactivity. | 2002 Aug 14 |
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Stable optically pure phosphino(silyl)carbenes: reagents for highly enantioselective cyclopropanation reactions. | 2004 Apr 19 |
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Syntheses, structures, luminescence and electrochemistry of benzene- and biphenyl-centered bis- and tris-1,3,2-diazaboroles and -1,3,2-diazaborolidines. | 2006 May 7 |
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Theoretical study of the hydroxylation of phenolates by the Cu(2)O (2)(N,N'-dimethylethylenediamine) (2) (2+) complex. | 2009 Feb |
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Reaction coordinate of a functional model of tyrosinase: spectroscopic and computational characterization. | 2009 May 13 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:13:50 GMT 2023
by
admin
on
Sat Dec 16 02:13:50 GMT 2023
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Record UNII |
6WAI8U5V0W
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Record Status |
Validated (UNII)
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