98139-95-8

Basic information

• Product Name: Cyclohexane, 1,2-dibromo-1-chloro-
• CAS NO: 98139-95-8
• Molecular Formula: C6H9Br2Cl
• Molecular Weight: 276.398
• Mol File: 98139-95-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexane, 1,2-dibromo-1-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 1,2-dibromo-1-chloro-(98139-95-8)
• EPA Substance Registry System: Cyclohexane, 1,2-dibromo-1-chloro-(98139-95-8)

Safety Data

• Hazardous Substances Data: 98139-95-8(Hazardous Substances Data)

Upstream product

• 930-66-5 1-chlorocyclohexene 
• 108-94-1 cyclohexanone 
• 67-66-3 chloroform 
• 7726-95-6 bromine 

Downstream Products

• 224316-65-8 (E)-3-(2-{(E)-2-[(1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxycarbonyl]-vinyl}-cyclohex-1-enyl)-acrylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester 
• 131496-57-6 1,2-bis[(E)-2-trimethylsilylethenyl]cyclohexene 
• 114493-71-9 1,2-diiodocyclohex-1-ene 
• 30984-03-3 cis-2,3-Diphenyl-2,3,5,6,7,8-hexahydro-naphthalin 
• 30984-01-1 1,2-(E,E)-distyrylcyclohexene 
• 930-66-5 1-chlorocyclohexene 
• 108-90-7 chlorobenzene 
• 87-82-1 hexabromobenzene 
• 55949-57-0 2-chloro-1,3-cyclohexadiene 
• 71-43-2 benzene 
• 20696-89-3 cyclohexene-d₂^1,2 
• 49676-92-8 1,2-dibromocyclohex-1-ene 

Relevant articles and documents

AROMATIC HETEROCYCLIC SUBSTITUTED OLEFIN COMPOUND, PREPARATION METHOD FOR SAME, PHARMACEUTICAL COMPOSITION OF SAME, AND APPLICATIONS THEREOF

Provided in the present application are an aromatic heterocyclic substituted olefin compound, a preparation method for same, a pharmaceutical composition of same, and applications thereof. The aromatic heterocyclic substituted olefin compound of the present invention is a novel ALK5 inhibitor and is for use in treating and/or preventing various ALK5-mediated diseases.

Auto-tandem catalysis: Synthesis of acridines by Pd-catalyzed C=C bond formation and C(sp2)-N cross-coupling

A facile palladium-catalyzed synthesis of acridines has been realized by consecutive C=C double bond formation and C-N cross-coupling. A variety of functionalized acridines can be accessed from easily available o-dihalobenzenes and N-tosylhydrazones in a single operation. This one-pot protocol has a wide scope with respect to both coupling partners, and provides an efficient route to functionalized acridine derivatives, which are generally difficult to synthesize by previously known methods.