25466-54-0

Basic information

• Product Name: 2-Octene, 1-bromo-
• CAS NO: 25466-54-0
• Molecular Formula: C8H15Br
• Molecular Weight: 191.111
• Mol File: 25466-54-0.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 2-Octene, 1-bromo-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Octene, 1-bromo-(25466-54-0)
• EPA Substance Registry System: 2-Octene, 1-bromo-(25466-54-0)

Safety Data

• Hazardous Substances Data: 25466-54-0(Hazardous Substances Data)

Upstream product

• 20739-58-6 2-octyn-1-ol 
• 628-17-1 amyl iodide 
• 628-71-7 1-Heptyne 
• 110-53-2 1-Bromopentane 
• 36602-98-9 2-(oct-2-yn-1-yloxy)tetrahydro-2H-pyran 
• 107691-96-3 (Z)-1-benzyloxy-2-octene 
• 16491-64-8 2-octin-1-yl acetate 
• 113120-16-4 Toluene-4-sulfonic acid (Z)-oct-2-enyl ester 
• 122712-60-1 (Z)-2-(oct-2-en-1-yloxy)tetrahydro-2H-pyran 
• 26001-58-1 (Z)-oct-2-en-1-ol 

Downstream Products

• 21944-96-7 (Z)-undec-5-en-2-one 
• 185057-99-2 oct-2-enyldiphenylphosphine oxide 
• 54844-65-4 (Z)-6-heneicosen-11-one 
• 91254-00-1 2,5-Undecadienal 
• 19689-18-0 4-decene 
• 74630-08-3 3-ethyl-1-octene 
• 1394257-31-8 (+/-)-(Z)-2-(benzyloxy)-1-(1-methyl-1H-imidazol-2-yl)dec-4-en-1-one 
• 1394257-24-9 (S,Z)-2-(benzyloxy)-1-(1-methyl-1H-imidazol-2-yl)dec-4-en-1-one 
• 1394257-32-9 (+/-)-(Z)-methyl 2-(benzyloxy)dec-4-enoate 
• 1394257-30-7 (S,Z)-methyl 2-(benzyloxy)dec-4-enoate 
• 1394257-23-8 (S,Z)-2-(benzyloxy)dec-4-enal 
• 1394257-22-7 (S,2E,6Z)-4-(benzyloxy)dodeca-2,6-dienal 
• 203742-72-7 [Fe(η(3)-n-C5H11CHCHCH2)(CO)(NO)(triphenyl phosphite)] 
• 203635-32-9 [Fe(η(3)-n-C5H11CHCHCH2)(CO)(NO)(triphenylphosphine)] 

Relevant articles and documents

5-F2t-isoprostane, a human hormone?

Syntheses of the four enantiomerically pure diastereomers of 5-F2t-isoprostane (5-8) are described. The key step is the lipase-catalyzed chemo-enzymatic resolution of the racemic diol 40 to give the mono-acetates 41 and 42. The enantiomerically

EXO- AND ENDOHORMONES, XVI SYNTHESIS OF (4E, 7Z)-4,7-TRIDECADIEN 1-YL ACETATE, THE SEX PHEROMONE FOR THE LEAFMINER LITHOCOLLETIS CORYLIFOLIELLA

The synthesis of the sex pheromone of the leafminer moth, Lithocolletis corylifoliella, (4E, 7Z)-4,7-tridecadien-1-yl acetate, was based on a C5+C8 scheme.The coupling reaction took place between the Grignard reagent of 4-pentin-1-1-oic acid and 1-bromo-2Z-octene.Propargylic alcohol was used as a starting material in order to obtain the two synthons.

PREPARATIVE SYNTHESIS OF TOSYLATES OF UNSATURATED ALCOHOLS AND UNSATURATED BROMIDES UNDER PHASE TRANSFER CONDITIONS

A preparative synthetic method has been developed for tosylates of unsaturated alcohols and their conversion to bromides under phase transfer conditions in the case of alkyn-1-ols, E- and Z-alken-1-ols, 3-methyl-3-buten-1-ol and cyclopropylmethanol.