CIS-STILBENEBORONIC ACID PINACOL ESTER

Base Information

Chemical Name:CIS-STILBENEBORONIC ACID PINACOL ESTER
CAS No.:264144-59-4
Molecular Formula:C20H23 B O2
Molecular Weight:306.212
Hs Code.:2931900090
Mol file:264144-59-4.mol

Synonyms:CIS-STILBENEBORONIC ACID PINACOL ESTER;cis-(1,2-Diphenylethenyl)boronic acid pinacol cyclic ester;cis-Stilbeneboronic acid pinacol cyclic ester

Suppliers and Price of CIS-STILBENEBORONIC ACID PINACOL ESTER

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
CIS-STILBENEBORONIC ACID PINACOL ESTER 99.00%
25G
$ 2338.88

American Custom Chemicals Corporation
CIS-STILBENEBORONIC ACID PINACOL ESTER 99.00%
10G
$ 1905.75

American Custom Chemicals Corporation
CIS-STILBENEBORONIC ACID PINACOL ESTER 99.00%
1G
$ 267.75

AHH
Cis-Stilbeneboronicacidpinacolester 99%
5g
$ 330.00

Total 10 raw suppliers

Chemical Property of CIS-STILBENEBORONIC ACID PINACOL ESTER

Chemical Property:

Vapor Pressure:2.52E-05mmHg at 25°C
Melting Point:92-94°C
Refractive Index:1.554
Boiling Point:369.5°Cat760mmHg
Flash Point:177.3°C
PSA：18.46000
Density:1.05g/cm³
LogP:4.85860

Purity/Quality:

99% ^*data from raw suppliers

CIS-STILBENEBORONIC ACID PINACOL ESTER 99.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 43
Safety Statements: 24/25-36/37

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of CIS-STILBENEBORONIC ACID PINACOL ESTER

There total 26 articles about CIS-STILBENEBORONIC ACID PINACOL ESTER which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 501-65-5
diphenyl acetylene

: 25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

: 264144-59-4
(Z)-1-(4',4',5',5'-tetramethyl-1’,3’,2’-dioxaborolan-2’-yl)-1,2-diphenylethene

Guidance literature:: With p-N,N-dimethylaminobenzoic acid; In octane; at 100 ℃; for 12h; Inert atmosphere;
DOI:10.1021/ol502285s

Reference yield: 95.0%

: 501-65-5
diphenyl acetylene

: 73183-34-3
bis(pinacol)diborane

: 264144-59-4
(Z)-1-(4',4',5',5'-tetramethyl-1’,3’,2’-dioxaborolan-2’-yl)-1,2-diphenylethene

Guidance literature:: With 1,3-bis(2,4,6-trimethylphenyl)imidazole-2-ylidene silver chloride; potassium tert-butylate; In tetrahydrofuran; methanol; at 50 ℃; for 5h; regioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1021/ol501465x

Reference yield: 71.0%

: 501-65-5
diphenyl acetylene

: 25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

: 1391743-16-0
(E)-1-(4',4',5',5'-tetramethyl-1’,3’,2’-dioxaborolan-2’-yl)-1,2-diphenylethene

: 264144-59-4
(Z)-1-(4',4',5',5'-tetramethyl-1’,3’,2’-dioxaborolan-2’-yl)-1,2-diphenylethene

Guidance literature:: With (carbonyl)(chloro)(hydrido)tris(triphenylphosphine)ruthenium(II); at 100 ℃; for 6h; Time; Temperature; stereoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1002/adsc.201800409