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141456-92-0

141456-92-0 | Ethanol, diamino- (9CI)

CAS No: 141456-92-0 Catalog No: AG001GF3 MDL No:

Product Description

Catalog Number:
AG001GF3
Chemical Name:
Ethanol, diamino- (9CI)
CAS Number:
141456-92-0
Molecular Formula:
C2H8N2O
Molecular Weight:
76.0977
IUPAC Name:
1,1-diaminoethanol
InChI:
InChI=1S/C2H8N2O/c1-2(3,4)5/h5H,3-4H2,1H3
InChI Key:
ZDTVBVUHESZSGN-UHFFFAOYSA-N
SMILES:
CC(O)(N)N

Properties

Complexity:
34.6  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
76.064g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
76.099g/mol
Monoisotopic Mass:
76.064g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
72.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.9  

Literature

Title Journal
Genome sequence of Desulfitobacterium hafniense DCB-2, a Gram-positive anaerobe capable of dehalogenation and metal reduction. BMC microbiology 20120101
Engineered protein nano-compartments for targeted enzyme localization. PloS one 20120101
Comparative analysis of carboxysome shell proteins. Photosynthesis research 20110901
Continuous wave photolysis magnetic field effect investigations with free and protein-bound alkylcobalamins. Journal of the American Chemical Society 20091202
Comparative genomic analyses of nickel, cobalt and vitamin B12 utilization. BMC genomics 20090101
Detection of biochemical pathways by probabilistic matching of phyletic vectors. PloS one 20090101
The pentameric vertex proteins are necessary for the icosahedral carboxysome shell to function as a CO2 leakage barrier. PloS one 20090101
Magnetic field effect studies indicate reduced geminate recombination of the radical pair in substrate-bound adenosylcobalamin-dependent ethanolamine ammonia lyase. Journal of the American Chemical Society 20071219
Computational investigation of hydrogen abstraction from 2-aminoethanol by the 1,5-dideoxyribose-5-yl radical: a model study of a reaction occurring in the active site of ethanolamine ammonia lyase. Chemistry (Weinheim an der Bergstrasse, Germany) 20040607
Computational study on mechanistic details of the aminoethanol rearrangement catalyzed by the vitamin B12-dependent ethanolamine ammonia lyase: His and Asp/Glu acting simultaneously as catalytic auxiliaries. The Journal of organic chemistry 20030905
Computational exploration of rearrangements related to the vitamin B12-dependent ethanolamine ammonia lyase catalyzed transformation. Journal of the American Chemical Society 20020731

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