(1S,2S)-(-)-N,N-Di-p-tosyl-1,2-cyclohexanediamine

• CAS: 212555-28-7
• Catalog Number: ACM212555287
• Category: Other Products
• Molecular Weight: 422.56
• Molecular Formula: C₂₀H₂₆N₂O₄S₂
• Synonyms: 212555-28-7, 482765_ALDRICH, CTK0J7803, ZINC00641928, AKOS015894766, AG-E-55834, I05-2747, (1S,2S)-(-)-N,N-Di-p-tosyl-1,2-cyclohexanediamine, Benzenesulfonamide, N,N-(1S,2S)-1,2-cyclohexanediylbis[4-methyl-, (1S,2S)-(-)-N,N inverted exclamation marka-Di-p-tosyl-1,2-cyclohexanediamine
• IUPAC Name: 4-methyl-N-[(1S,2S)-2-[(4-methylphenyl)sulfonylamino]cyclohexyl]benzenesulfonamide
• SMILES: CC1=CC=C(C=C1)S(=O)(=O)NC2CCCCC2NS(=O)(=O)C3=CC=C(C=C3)C
• InChI Key: FIAAGQKYVFEMGC-PMACEKPBSA-N
• Melting Point: 170-173ºC(lit.)
• Exact Mass: 422.13300
• H-Bond Acceptor: 6
• H-Bond Donor: 2

Synthetic Use

Upstream Synthesis Route 1

• 21436-03-3
• 98-59-9

• 212555-28-7

Reference: [1]Hilgraf, Robert; Pfaltz, Andreas
[Advanced Synthesis and Catalysis, 2005, vol. 347, # 1, p. 61 - 77]
[2]Golding, Simon W.; Hambley, Trevor W.; Lawrance, Geoffrey A.; Luther, Stephan M.; Maeder, Marcel; Turner, Peter
[Journal of the Chemical Society, Dalton Transactions, 1999, # 12, p. 1975 - 1980]

Upstream Synthesis Route 2

• 98-59-9
• 191480-65-6

• 212555-28-7

Reference: [1]Alfonso, Ignacio; Astorga, Covadonga; Rebolledo, Francisca; Gotor, Vicente
[Tetrahedron Asymmetry, 1999, vol. 10, # 13, p. 2515 - 2522]

Downstream Synthesis Route 1

• 16695-22-0
• 212555-28-7

• 929078-51-3

Reference: [1]Journal of the Chemical Society, Dalton Transactions,1999,p. 1975 - 1980

* For details of the synthesis route, please refer to the original source to ensure accuracy.