507989-55-1

Basic information

• Product Name: 4,4-bis(benzyloxycarbonyl)-1,7-dimethylhepta-1,6-diyne
• Synonyms: 4,4-bis(benzyloxycarbonyl)-1,7-dimethylhepta-1,6-diyne
• CAS NO: 507989-55-1
• Molecular Weight: 388.463
• Mol File: 507989-55-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4,4-bis(benzyloxycarbonyl)-1,7-dimethylhepta-1,6-diyne(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-bis(benzyloxycarbonyl)-1,7-dimethylhepta-1,6-diyne(507989-55-1)
• EPA Substance Registry System: 4,4-bis(benzyloxycarbonyl)-1,7-dimethylhepta-1,6-diyne(507989-55-1)

Safety Data

• Hazardous Substances Data: 507989-55-1(Hazardous Substances Data)

Upstream product

• 15014-25-2 malonic acid dibenzyl ester 
• 3355-28-0 1-Bromo-2-butyne 

Downstream Products

• 1401322-71-1 dibenzyl 3-(cyanomethyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)dicarboxylate 
• 1401322-75-5 dibenzyl 3-(4-cyanophenyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate 
• 1401322-76-6 (E)-dibenzyl 3-(2-cyanovinyl)-1,4-dimethyl-5Hcyclopenta[c]pyridine-6,6(7H)-dicarboxylate 
• 1401322-79-9 dibenzyl 3-(2-cyanoethyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate 
• 1401322-80-2 dibenzyl 3-(chloromethyl)-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate 
• 1401322-83-5 6,6-dibenzyl 3-ethyl 1,4-dimethyl-5H-cyclopenta[c]pyridine-3,6,6(7H)-tricarboxylate 
• 1401322-85-7 dibenzyl 3-benzoyl-1,4-dimethyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate 
• 1401322-87-9 dibenzyl 1,4-dimethyl-3-phenyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate 
• 1401322-88-0 dibenzyl 1,4-dimethyl-3-p-tolyl-5H-cyclopenta[c]pyridine-6,6(7H)-dicarboxylate 
• 1437300-37-2 dibenzyl 2-((1-benzyl-4,5-dimethyl-1H-pyrrol-3-yl)methyl)-2-(but-2-yn-1-yl)malonate 
• 1607479-71-9 1,4-dimethyl-2-p-tolyl-3-p-tolylimino-2,3,5,7-tetrahydro[2]pyridine-6,6-dicarboxylic acid dibenzyl ester 
• 1607479-83-3 1,4-dimethyl-3-oxo-3,5-dihydro-7H-cyclopenta[c]pyran-6,6-dicarboxylic acid dibenzyl ester 

Relevant articles and documents

Cycloisomerization of dienes and enynes catalysed by a modified ruthenium carbene species

Cycloisomerization is a totally atom economic procedure which converts dienes and enynes into cyclic molecules. Modification of Grubbs' 2nd generation catalysts by reaction with dimethylformamide provides a new species able to catalyse this transformation