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TRANS-2-(4-METHOXYPHENYL)-

CAS No.
72316-18-8
Chemical Name:
TRANS-2-(4-METHOXYPHENYL)-
Synonyms
TRANS-2-(4-METHOXYPHENYL)-;(E)-(4-Methoxystyryl)boronic acid;[(E)-2-(4-Methoxyphenyl)ethenyl]boronic acid;(E)-2-(4-METHOXYPHENYL)ETHENYL-1-BORONIC ACID;trans-2-(4-Methoxyphenyl)vinylboronic acid >=95%;Boronic acid, B-[(1E)-2-(4-methoxyphenyl)ethenyl]-
CBNumber:
CB2499545
Molecular Formula:
C9H11BO3
Molecular Weight:
177.99
MDL Number:
MFCD04039879
MOL File:
72316-18-8.mol
MSDS File:
SDS
Last updated:2022-12-30 16:20:48

TRANS-2-(4-METHOXYPHENYL)- Properties

Melting point 140-144 °C(lit.)
Boiling point 373.1±44.0 °C(Predicted)
Density 1.149±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 9.61±0.43(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
WGK Germany  3
HS Code  2931900090

TRANS-2-(4-METHOXYPHENYL)- price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 518980 trans-2-(4-Methoxyphenyl)vinylboronic acid ≥95% 72316-18-8 1g $150 2024-03-01 Buy
Sigma-Aldrich 518980 trans-2-(4-Methoxyphenyl)vinylboronic acid ≥95% 72316-18-8 10g $895 2024-03-01 Buy
American Custom Chemicals Corporation BOR0001739 TRANS-2-(4-METHOXYPHENYL)VINYLBORONIC ACID 95.00% 72316-18-8 10G $1720.9 2021-12-16 Buy
American Custom Chemicals Corporation BOR0001739 TRANS-2-(4-METHOXYPHENYL)VINYLBORONIC ACID 95.00% 72316-18-8 1G $203.7 2021-12-16 Buy
Crysdot CD12039578 (E)-(4-Methoxystyryl)boronicacid 95+% 72316-18-8 10g $440 2021-12-16 Buy
Product number Packaging Price Buy
518980 1g $150 Buy
518980 10g $895 Buy
BOR0001739 10G $1720.9 Buy
BOR0001739 1G $203.7 Buy
CD12039578 10g $440 Buy

TRANS-2-(4-METHOXYPHENYL)- Chemical Properties,Uses,Production

Uses

Reactant involved in:• ;Enantioselective conjugate addition reactions with indole-appended enones1• ;Liebeskind-Srogl cross-coupling reactions2• ;Petasis asymmetric dihydroxylation for synthesis of (dihydroxy)homotyrosines3• ;Copper-catalyzed trifluoromethylation4• ;Asymmetric Michael addition with hydroxycinnamaldehydes5• ;Cobalt-catalyzed coupling for synthesis of phenylbutenylheteroarenes6

Uses

Reactant involved in:

  • Enantioselective conjugate addition reactions with indole-appended enones
  • Liebeskind-Srogl cross-coupling reactions
  • Petasis asymmetric dihydroxylation for synthesis of (dihydroxy)homotyrosines
  • Copper-catalyzed trifluoromethylation
  • Asymmetric Michael addition with hydroxycinnamaldehydes
  • Cobalt-catalyzed coupling for synthesis of phenylbutenylheteroarenes

TRANS-2-(4-METHOXYPHENYL)- Preparation Products And Raw materials

Raw materials

Preparation Products

TRANS-2-(4-METHOXYPHENYL)- Suppliers

Global( 29)Suppliers
Supplier Tel Email Country ProdList Advantage
Wuhan Chemwish Technology Co., Ltd
027-67849912 sales@chemwish.com CHINA 10821 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131957 58
Energy Chemical 021-021-58432009 400-005-6266 sales8178@energy-chemical.com China 44688 61
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35896 56
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42958 64
Syntechem Co.,Ltd info@syntechem.com China 12984 57
Tianjin heowns Biochemical Technology Co., Ltd. 400 638 7771 sales@heowns.com China 14435 57
Nanjing Norris-Pharm Technology Co., Ltd 13901585132 799750417@qq.com China 8878 55
9ding chemical ( Shanghai) Limited 4009209199 sales@9dingchem.com China 18209 56
TRANS-2-(4-METHOXYPHENYL)- (E)-2-(4-METHOXYPHENYL)ETHENYL-1-BORONIC ACID [(E)-2-(4-Methoxyphenyl)ethenyl]boronic acid (E)-(4-Methoxystyryl)boronic acid trans-2-(4-Methoxyphenyl)vinylboronic acid >=95% Boronic acid, B-[(1E)-2-(4-methoxyphenyl)ethenyl]- 72316-18-8 CH3OC6H4CHCHBOH2 Alkenyl Boronic Acids Boronic Acids Boronic Acids and Derivatives Chemical Synthesis Organometallic Reagents Alkenyl Boronic Acids Boronic Acids and Derivatives blocks BoronicAcids