62614-72-6

Basic information

• Product Name: 2-Hexene, 6-chloro-, (E)-
• CAS NO: 62614-72-6
• Molecular Formula: C6H11Cl
• Molecular Weight: 118.606
• Mol File: 62614-72-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Hexene, 6-chloro-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Hexene, 6-chloro-, (E)-(62614-72-6)
• EPA Substance Registry System: 2-Hexene, 6-chloro-, (E)-(62614-72-6)

Safety Data

• Hazardous Substances Data: 62614-72-6(Hazardous Substances Data)

Upstream product

• 28077-73-8 6-chlorohex-2-yne 
• 928-93-8 4-hexyn-1-ol 
• 6126-50-7 hex-4-en-1-ol 
• 928-89-2 6-chlorohexene 
• 14267-92-6 1-chloro-4-pentyne 
• 928-91-6 (Z)-4-hexenol 
• 629-11-8 1,6-hexanediol 
• 821-41-0 5-Hexen-1-ol 
• 928-92-7 (E)-hex-4-en-1-ol 

Downstream Products

• 70681-89-9 ((E)-3-Hex-4-enyl)-cyclohex-2-enol 
• 2931-10-4 2-ethylcyclopent-2-en-1-one 
• 1121-18-2 2-methyl-2-cyclohexen-1-one 
• 105-21-5 4-propylbutanolide 
• 70681-91-3 3-<(E)-4-hexenyl>-2-cyclohexen-1-one 

Relevant articles and documents

Site-selective catalytic deaminative alkylation of unactivated olefins

A catalytic deaminative alkylation of unactivated olefins is described. The protocol is characterized by its mild conditions, wide scope - including the use of ethylene as substrate -, and exquisite site-selectivity pattern for both a-olefins and internal olefins, thus unlocking a new catalytic platform to forge sp3-sp3 linkages, even in the context of late-stage functionalization.

Diastereoselective cycloisomerizations of enediynes via palladium catalysis

Considerations of atom economy drive a search for reactions that are simple additions which, performed intramolecularly, are cycloisomerizations. Exposure of acyclic enediynes to a catalyst generated by mixing a Pd(0) complex with acetic acid normally in

Photochemistry of N-Alk-4-enyl and N-Alk-5-enyl-phthalimides: Two Different Types of Cyclization Reaction

Photochemical reactions of N-alk-4- and -5-enylphthalimides (1a-e) have been investigated.In the photolyses of acetonitrile solutions of (1a-e), intramolecular cyclization reactions accompanying C(=O)-N bond cleavage to give (2a-e) were generally predominant, together with intramolecular hydrogen abstraction in some cases.Photolyses of cis- and trans-N-hex-4-enylphthalimides in acetonitrile solution showed stereospecific cyclization reactions; irridiation of cis-(1e) gave cis-(2e) and that of trans-(1e) gave trans-(2e) selectively with low conversion.In methanol (1d), which has a vinyl ether moiety, gave different types of cyclization product: namely, (8a) and (9a), methanol-incorporated products probably resulting from an intramolecular electron transfer process.