1,2-Diaminocyclohexane

1,2-Diaminocyclohexane Basic information
Product Name:1,2-Diaminocyclohexane
Synonyms:1,2-DIAMINOCYCLOHEXANE;(1R,2R)-(-)-1,2-CYCLOHEXANEDIAMINE;(1R)-TRANS-1,2-CYCLOHEXANEDIAMINE;(1R)-(-)-TRANS-1,2-DIAMINOCYCLOHEXANE;(1R)-TRANS-1,2-DIAMINOCYCLOHEXANE;1,2-Cylohexanediamine;1,2-Diaminocyclohexane,c&t;1,2-diaMinocylohexane
CAS:694-83-7
MF:C6H14N2
MW:114.19
EINECS:211-776-7
Product Categories:
Mol File:694-83-7.mol
1,2-Diaminocyclohexane Structure
1,2-Diaminocyclohexane Chemical Properties
Melting point 41-45 °C
Boiling point 92-93 °C18 mm Hg(lit.)
density 0.931 g/mL at 25 °C(lit.)
vapor pressure 0.4 mm Hg ( 20 °C)
refractive index n20/D 1.49(lit.)
Fp 169 °F
storage temp. 2-8°C
form Liquid
pka10.76±0.70(Predicted)
color Clear
PH11.3 (5g/l, H2O, 20℃)neutral
Water Solubility miscible
Sensitive Air Sensitive
BRN 506142
LogP0 at 20℃
CAS DataBase Reference694-83-7(CAS DataBase Reference)
NIST Chemistry Reference1,2-Cyclohexanediamine(694-83-7)
EPA Substance Registry System1,2-Cyclohexanediamine (694-83-7)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3259 8/PG 2
WGK Germany 3
RTECS GU8749500
34
TSCA Yes
HazardClass 8
PackingGroup III
HS Code 29213099
Hazardous Substances Data694-83-7(Hazardous Substances Data)
MSDS Information
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1,2-Diaminocyclohexane English
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1,2-Diaminocyclohexane Usage And Synthesis
Chemical Propertiesclear slightly yellow to yellow liquid
Uses1,2-Diaminocyclohexane was used in the synthesis of chiral ruthenium(IV)-oxo complexes.
Usessuzuki reaction
Uses1,2-Diaminocyclohexane was used in the synthesis of chiral ruthenium(IV)-oxo complexes & bicyclic pyrazine derivatives.
DefinitionChEBI: Cyclohexane-1,2-diamine is a primary aliphatic amine.
General Description1,2-Diaminocyclohexane undergoes non-templated reaction with homochiral as well as the racemic form of trans-1,2-diaminocyclohexane with terephthaldehyde to yield (3+3)-cyclocondensed molecular triangles. It acts as ligand and forms organotin complexes, having potential applications as metal-based antitumour drugs.
Flammability and ExplosibilityNonflammable
1,2-Diaminocyclohexane Preparation Products And Raw materials
Preparation ProductsOxaliplatin-->(9-(4-IODOPHENYL))-9H-CARBAZOLE-->CDTA-->3A-METHYL-DECAHYDRO-BENZO[D]PYRROLO[1,2-A]-IMIDAZOL-1-ONE
1,2-CYCLOHEXANEDIAMINE SULFATE TRANS-1,2-DIAMINOCYCLOHEXANE SULFATE 1,4-DIMETHOXYOCTAHYDROQUINOXALINE-2,3-DIONE DECAHYDRO-QUINOXALINE (-)-(1S,2R)-CIS-3,4-DICHLORO-N-METHYL-N-[2-(1-PYRROLIDINYL)-CYCLOHEXYL]-BENZENEACETAMIDE TARTRATE CIS-OCTAHYDRO-2H-BENZIMIDAZOL-2-ONE (R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE (1S,2S)-(-)-1,2-Diaminocyclohexane L-tartrate (1R,2R)-(+)-1,2-CYCLOHEXANEDIAMINE L-TARTRATE (+)-U-50488 HYDROCHLORIDE 1,5-BIS(TRIMETHYLSILYL)-4.8-METHANOHEXAHYDROBENZO(1,2D-4,5D)BISTRIAZOLE TRANS-1,2-DIAMINOCYCLOHEXANE-N,N,N -TETRAACETIC ACID,trans-1,2-DIAMINOCYCLOHEXANE-N,N,N,N TETRRAACETIC ACID extrapure AR 1,2-BIS(HYDROXYAMINO)CYCLOHEXANE (1,2-Diaminocyclohexane)platinum() chloride,(1,2-DIAMINOCYCLOHEXANE)PLATINUM(II) CHLORIDE (+/-)-(5ALPHA,7ALPHA,8BETA)-3,4-DICHLORO-N-METHYL-N-(7-[1-PYRROLIDINYL]-1-OXASPIRO[4.5]DEC-8-YL)BENZENEACETAMIDE MESYLATE (-)-U-50488 HYDROCHLORIDE 1,3-DIHYDROXY-2-CARBOXYPERHYDROBENZIMIDAZOLE ETHANOLATE CDTA DISODIUM SALT

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