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2592-73-6

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2592-73-6 Usage

Appearance

Colorless, crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Reagent in organic synthesis
b. Building block for creating other compounds
c. Reactant in the synthesis of polymers
d. Precursor to flame retardants

Safety precautions

a. Potential skin and eye irritant
b. Harmful if inhaled or ingested
c. Handle with caution
d. Store and handle in a well-ventilated area
e. Use personal protective equipment when working with it to minimize potential health risks

Check Digit Verification of cas no

The CAS Registry Mumber 2592-73-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2592-73:
(6*2)+(5*5)+(4*9)+(3*2)+(2*7)+(1*3)=96
96 % 10 = 6
So 2592-73-6 is a valid CAS Registry Number.

2592-73-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-dibromo-1-phenylethenyl)benzene

1.2 Other means of identification

Product number -
Other names 1,1-Dibrom-2,2-diphenyl-aethen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2592-73-6 SDS

2592-73-6Relevant articles and documents

Assembly of organosilver coordination frameworks with aromatic ligands bearing a terminal enediyne group

Hau, Sam C.K.,Mak, Thomas C.W.

, p. 63 - 72 (2013)

In a series of five silver(I) complexes synthesized with (2-ethynylbut-1-en-3-yne-1,1-diyl)dibenzene (H2L1) and 9-(penta-1,4-diyn-3-ylidene)-9H-fluorene (H2L2), each resulting ethynide ligand is invariably inserted into a Agn/s

Sandwich and half-sandwich metal complexes derived from cross-conjugated 3-methylene-penta-1,4-diynes

Vincent, Kevin B.,Gluyas, Josef B. G.,Zeng, Qiang,Yufit, Dmitry S.,Howard, Judith A. K.,Hartl, Franti?ek,Low, Paul J.

, p. 5522 - 5531 (2017)

The cross-conjugated ethynyl-vinylidene [Ph2CC(CCH){C(H)CRu(PPh3)2Cp}]PF6 ([4a]PF6), and [FcC(H)C(CCH){C(H)CRu(PPh3)2Cp}]PF6 ([4b]PF6), and ethynyl-alkynyl Ph2CC(CCH){CCRu(PPh3)2Cp} (5a), and FcC(H)C(CCH){CCRu(PPh3)2Cp} (5b) compounds (Cp = η5-cyclopentadienyl) have been prepared from reactions of the known 3-methylene-penta-1,4-diynes Ph2CC(CCH)2 (3a) and [FcCHC(CCH)2] (3b) with [RuCl(PPh3)2Cp]. The compounds derived from 3b incorporating the more electron-rich alkene proved to be unstable during work-up, and attempts to prepare bis(ruthenium) complexes from 3a and 3b or from transmetallation reactions of the bis(alkynylgold) complex FcCHC(CCAuPPh3)2 (7) with RuCl(PPh3)2Cp were unsuccessful. The related bis-and tris(ferrocenyl) derivatives Ph2CC(CCFc)2 (6a) and FcCHC(CCFc)2 (6b) were more readily obtained from Pd(ii)/Cu(i) catalysed cross-coupling reactions of FcCCH with the 1,1-dibromo vinyl complexes PhCCBr2 (1a) and FcC(H)CBr2 (1b). Cyclic voltammetry of 6a and 6b using n-Bu4N[PF6] as the supporting electrolyte shows broad, overlapping waves arising from the sequential oxidation of the ferrocenyl moieties in electronically and chemically similar environments. Electrostatic effects between the ferrocenyl moieties are enhanced in solutions of the weakly ion-pairing electrolyte n-Bu4N[B{C6H3(CF3)2-3,5}4], leading to better resolution of the individual electrochemical processes. The comparative IR spectroelectrochemical response of 6a and 6b suggest the vinyl ferrocene moiety in 6b undergoes oxidation before the ethynyl ferrocene fragments. There is no evidence of electronic coupling between the metallocene moieties and [6a]+, [6b]n+ (n = 1, 2) are best described as Class I mixed-valence compounds.

Photo-activated I-type photosensitizer as well as preparation method and application thereof

-

Paragraph 0047-0052, (2021/08/06)

The invention belongs to the technical field of biological imaging treatment materials, and discloses a photo-activated I-type photosensitizer as well as a preparation method and application thereof. The photo-activated I-type photosensitizer has a struct

Photoinduced crystallization isoquinoline salt compound, preparation method and application thereof, and preparation method of nanocrystal

-

Paragraph 0060; 0064; 0065, (2020/12/30)

The invention belongs to the technical field of photoresponse materials, and discloses a photoinduced crystallization isoquinoline salt compound, a preparation method and application thereof, and a preparation method of nanocrystals, and the preparation m

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