1586-98-7

Basic information

• Product Name: Benzene, (2,3-dibromopropyl)-
• CAS NO: 1586-98-7
• Molecular Formula: C9H10Br2
• Molecular Weight: 277.986
• Mol File: 1586-98-7.mol
• Article Data: 27

Chemical Properties

• CAS DataBase Reference: Benzene, (2,3-dibromopropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (2,3-dibromopropyl)-(1586-98-7)
• EPA Substance Registry System: Benzene, (2,3-dibromopropyl)-(1586-98-7)

Safety Data

• Hazardous Substances Data: 1586-98-7(Hazardous Substances Data)

Upstream product

• 300-57-2 allylbenzene 
• 67-56-1 methanol 
• 4436-24-2 1,2-epoxy-3-phenylpropane 
• 71-43-2 benzene 
• 64-17-5 ethanol 
• 873-49-4 cyclopropylbenzene 

Downstream Products

• 63888-20-0 3-phenyl-1-propen-1-yl acetate 
• 33962-91-3 N,N-diethyl-3-phenylprop-2-en-1-amine 
• 673-32-5 1-Phenylprop-1-yne 
• 2327-99-3 1-phenylpropadiene 
• 167315-39-1 Ni(1,2-bis(2-mercaptophenylthio)-3-phenylpropanoato^(2-)) 
• 10147-11-2 propargyl benzene 
• 859944-01-7 (3-bromo-allyl)-benzene 
• 21040-45-9 Cinnamyl acetate 
• 116518-89-9 (E)-cinnamyl tetradecanoate 
• 34994-60-0 (2E)-3-phenylprop-2-en-1-yl 4-nitrobenzoate 
• 119793-72-5 (E)-2-(3-phenyl-allyl) malonic acid dimethyl ester 
• 63082-55-3 diethyl (E)-cinnamyl malonate 
• 1338926-17-2 (E)-ethyl 2-nitro-5-phenylpent-4-enoate 
• 17480-07-8 2-[(E)-3-phenylprop-2-enyl]-2,3-dihydro-1H-isoindole-1,3-dione 

Relevant articles and documents

Synthesis and extraction properties of oxathiacrown compounds containing benzyl groups

8-Benzyl-1.4-dioxa-7,10-dithiacyclododecane and 11-benzyl-1,4,7-trioxa-10, 13-dithiacyclopentadecane were obtained by the interaction of (2,3-dibromo-1-propyl)benzene with 1,8-dimercapto-3,6-dioxaoctane and 1,11-dimercapto-3,6,9-trioxaundecane. The extrac

Dibrominated addition and substitution of alkenes catalyzed by Mn2(CO)10

A practical method for the dibromination of alkenes without using molecular bromine is consistently appealing in organic synthesis. Herein, we report Mn-catalyzed dibrominated addition and substitution of alkenes only with N-bromosuccinimide, producing a variety of synthetically valuable dibrominated compounds in moderate to high yields. This journal is

A Highly Efficient Method for the Bromination of Alkenes, Alkynes and Ketones Using Dimethyl Sulfoxide and Oxalyl Bromide

The pairing of DMSO and oxalyl bromide is reported as a highly efficient brominating reagent for various alkenes, alkynes and ketones. This bromination approach demonstrates remarkable advantages, such as mild conditions, low cost, short reaction times, provides excellent yields in most cases and represents a very attractive alternative for the preparation of dibromides and α-bromoketones.

Closing the Gap: Structural Evidence for the Missing Hexabromide Dianion [Br6]2?

The formation and experimental characterization of the first hexabromide dianion is presented. This dianion fills the last remaining gap in the series of polybromides from the tribromide [Br3]? to the undecabromide [Br11]