(+/-)-trans-1,2-Diaminocyclohexane
(+/-)-trans-1,2-Diaminocyclohexane Basic information
- Product Name:
- (+/-)-trans-1,2-Diaminocyclohexane
- Synonyms:
-
- TIMTEC-BB SBB007639
- (+/-)-TRANS-1,2-CYCLOHEXANEDIAMINE
- TRANS-1,2-CYCLOHEXANEDIAMINE
- 1,2-Cyclohexanediamine, trans-
- trans-1,2-Cyclohexaneiamine
- Cyclohexanediamine
- Trans-(L)-1,2-Diaminecyclohexane
- trans-1,2-Diaminocyclohexane(Racemic)
- CAS:
- 1121-22-8
- MF:
- C6H14N2
- MW:
- 114.19
- EINECS:
- 601-163-6
- Product Categories:
-
- bc0001
- Mol File:
- 1121-22-8.mol
(+/-)-trans-1,2-Diaminocyclohexane Chemical Properties
- Melting point:
- 14-15 °C(lit.)
- Boiling point:
- 79-81 °C15 mm Hg(lit.)
- Density
- 0.951 g/mL at 25 °C(lit.)
- vapor pressure
- 0.4 mm Hg ( 20 °C)
- refractive index
- n20/D 1.489(lit.)
- Flash point:
- 156 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Liquid
- pka
- 9.94(at 20℃)
- color
- Clear colorless to light yellow
- Water Solubility
- Soluble
- Sensitive
- Air Sensitive
- BRN
- 506142
- InChIKey
- SSJXIUAHEKJCMH-WDSKDSINSA-N
- CAS DataBase Reference
- 1121-22-8(CAS DataBase Reference)
- NIST Chemistry Reference
- trans-1,2-Cyclohexanediamine(1121-22-8)
- EPA Substance Registry System
- 1,2-Cyclohexanediamine, (1R,2R)-rel- (1121-22-8)
Safety Information
- Hazard Codes
- C
- Risk Statements
- 34
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN 2735 8/PG 2
- WGK Germany
- 3
- F
- 10-34
- TSCA
- Yes
- HazardClass
- 8
- PackingGroup
- II
- HS Code
- 29213000
MSDS
- Language:English Provider:(+/-)-trans-1,2-Cyclohexanediamine
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
(+/-)-trans-1,2-Diaminocyclohexane Usage And Synthesis
Chemical Properties
clear colorless to light yellow liquid
Uses
(^+)-trans-1,2-Diaminocyclohexane is employed in the synthesis of macrocyclic [3+3] hexa Schiff base. It also plays an important role in the preparation of multidentate ligands, chiral auxiliaries and chiral stationary phases. Further, it is used to prepare [2+2] macrocyclization by reacting with aliphatic dialdehydes. In addition to this, it acts as a chiral ligand, which finds application in asymmetric catalysis.
Uses
(±)-trans-1,2-Diaminocyclohexane was used in the synthesis of macrocyclic [3+3] hexa Schiff base. It was also employed in the synthesis of multidentate ligands, chiral auxiliaries and chiral stationary phases.
General Description
(±)-trans-1,2-Diaminocyclohexane was condensed with aliphatic dialdehydes to form [3+3] or [2+2] macrocyclization products.
Purification Methods
Purify and store the diamine as for the cis-isomer above as it is a strong base and becomes yellow on storage. [Beilstein 13 IV 1.]
(+/-)-trans-1,2-Diaminocyclohexane Preparation Products And Raw materials
Preparation Products
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(+/-)-trans-1,2-Diaminocyclohexane(1121-22-8)Related Product Information
- 1,2-Cyclohexanedione
- Hexamethylenediamine
- 1,2-Cyclohexanediol
- TRANS-1,4-DIAMINOCYCLOHEXANE
- trans,trans-2,4-Undecadienal
- TRANS-1,4-CYCLOHEXANEDIOL
- trans-1,2-Cyclopentanediol
- (E)-1,4-Dibromobut-2-ene
- TRANS-CYCLOBUTANE-1,2-DICARBOXYLIC ACID
- trans-1,4-Cyclohexanedicarboxybic acid
- TRANS-1,2-CYCLOHEXANEDIOL
- rich_d_transallethrin
- (1R)-TRANS-1,2-DIAMINOCYCLOHEXANE,(1R)-(-)-TRANS-1,2-DIAMINOCYCLOHEXANE
- Enadoline
- (1S,2S)-(-)-1,2-DIAMINOCYCLOHEXANE-N,N'-BIS(2'-DIPHENYLPHOSPHINOBENZOYL)
- (1S,2S)-(+)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]ALUMINUM (III) CHLORIDE
- (S,S)-(+)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-COBALT(II)
- (1S)-TRANS-1,2-DIAMINOCYCLOHEXANE D-TARTRATE