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263761

Sigma-Aldrich

trans-4-Aminocyclohexanol hydrochloride

97%

Synonym(s):

trans-4-Hydroxycyclohexylamine hydrochloride

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About This Item

Linear Formula:
H2NC6H10OH · HCl
CAS Number:
50910-54-8
Molecular Weight:
151.63
Beilstein/REAXYS Number:
3909294
MDL number:
MFCD00012566
UNSPSC Code:
12352100
PubChem Substance ID:
24855994
NACRES:
NA.22

Quality Level

100

assay

97%

mp

225-227 °C (lit.)

SMILES string

Cl.N[C@H]1CC[C@H](O)CC1

InChI

1S/C6H13NO.ClH/c7-5-1-3-6(8)4-2-5;/h5-6,8H,1-4,7H2;1H/t5-,6-;

InChI key

RKTQEVMZBCBOSB-KYOXOEKESA-N

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Application

trans-4-Aminocyclohexanol hydrochloride has been used in the synthesis of:
  • N-substituted 7-azabicyclo[2.2.1]heptanes via transannular nucleophilic displacement
  • trans-4-methoxyoxalamido-1-cyclohexanol
  • benzoxazine, required for the preparation of polybenzoxazine-silica hybrid nanocomposites

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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N N Polushin
Nucleic acids research, 28(16), 3125-3133 (2000-08-10)
Synthesis of new terminus modifiers, bearing, along with a phosphoramidite moiety, one, two or four methoxyoxalamido (MOX) precursor groups, is described. These modifiers are introduced onto the 5'-end of a synthetic oligodeoxyribonucleotide as the last step of an automated synthesis
D M Creasy et al.
Experimental and molecular pathology, 52(2), 155-169 (1990-04-01)
Male Wistar strain rats were fed a diet providing an intake of 0 or 400 mg cyclohexylamine (CHA)/kg body weight/day for 1, 3, 7, 9, or 13 weeks. At the end of the appropriate feeding period the rats were perfused-fixed
Dwayne A Dias et al.
Organic letters, 11(16), 3694-3697 (2009-07-28)
The intramolecular variant of the homo-[3 + 2]-dipolar cycloaddition of nitrones (generated in situ from an aldehyde and a hydroxylamine) with donor-acceptor cyclopropanes allows for the efficient synthesis of bridged tetrahydro-1,2-oxazines. This domino sequence produces adducts amenable to reductive N-O
Polybenzoxazine-silica (PBZ-SiO2) hybrid nanocomposites through in situ sol-gel method.
Devaraju S, et al.
Journal of Sol-Gel Science and Technology, 60(1), 33-40 (2011)
Synthesis and microbial hydroxylation of some azabicycloalkanes.
Olivo HF, et al.
Tetrahedron Letters, 39(11), 1309-1312 (1998)

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