141276-61-1

Basic information

• Product Name: (2α,5α)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinone
• CAS NO: 141276-61-1
• Molecular Weight: 564.766
• Mol File: 141276-61-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2α,5α)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinone(CAS DataBase Reference)
• NIST Chemistry Reference: (2α,5α)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinone(141276-61-1)
• EPA Substance Registry System: (2α,5α)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinone(141276-61-1)

Safety Data

• Hazardous Substances Data: 141276-61-1(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 141276-59-7 (2α,4α,5β)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinol 
• 141276-58-6 (2α,5β)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-1,2,3,6-tetrahydro-2-tridecylpyridine 
• 141276-57-5 (2α,5β)-(+/-)-1-benzyloxycarbonyl-1,2,3,6-tetrahydro-5-trichloroacetamino-2-tridecylpyridine 
• 141276-56-4 (2α,3β)-(+/-)-1-benzyloxycarbonyl-1,2,3,6-tetrahydro-2-tridecyl-3-pyridinol 
• 141276-65-5 2-Tridecyl-2H-pyridine-1-carboxylic acid benzyl ester 
• 59020-06-3 4-trimethylstannyl-pyridine 
• 765-09-3 1-bromotridecane 
• 141276-61-1 (2R,5S)-5-Benzyloxycarbonylamino-4-oxo-2-tridecyl-piperidine-1-carboxylic acid benzyl ester 

Downstream Products

• 141276-59-7 (2α,4β,5β)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinol 
• 141276-61-1 (2α,5α)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinone 
• 141276-59-7 (2α,4α,5α)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinol 
• 141276-59-7 (2α,4β,5α)-(+/-)-1-benzyloxycarbonyl-5-benzyloxycarbonylamino-2-tridecyl-4-piperidinol 

Relevant articles and documents

SYNTHESIS OF (+/-)-TETRAHYDROPSEUDODISTOMIN, A HYDROGENATION PRODUCT OF ANTINEOPLASTIC ALKALOIDS, PSEUDODISTOMINS A AND B

2-Alkyl-1,2,3,6-tetrahydro-3-pyridinols (6, R2 = H) with trans arrangement of the side chains were prepared by sodium cyanoborohydride reduction of the singlet oxygen adducts (5) of 1,2-dihydropyridine derivatives (4) in the presence of tin(II) chloride.S