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trans-1-Hepten-1-ylboronic acid pinacol ester

CAS No.
169339-75-7
Chemical Name:
trans-1-Hepten-1-ylboronic acid pinacol ester
Synonyms
1-HEPTENYL-1-BORONIC ACID, PINACOL ESTER;TRANS-1-HEPTENYLBORONIC ACID PINACOL ESTER;TRANS-1-HEPTENYL-1-BORONIC ACID PINACOL ESTER;trans-1-Hepten-1-ylboronic acid pinacol ester 97%;trans-1-Hepten-1-ylboronic acid pinacol ester, 97%;E-2-(1-HEPTENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE;2-[(E)-hept-1-enyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;TRANS-4,4,5,5-TETRAMETHYL-2-HEPT-1-ENYL-1,3,2-DIOXABOROLANE;1,3,2-Dioxaborolane, 2-(1E)-1-hepten-1-yl-4,4,5,5-tetramethyl-;(E)-2-(Hept-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CBNumber:
CB6776048
Molecular Formula:
C13H25BO2
Molecular Weight:
224.15
MDL Number:
MFCD05663884
MOL File:
169339-75-7.mol
MSDS File:
SDS
Last updated:2022-08-23 14:33:43

trans-1-Hepten-1-ylboronic acid pinacol ester Properties

Boiling point 73-77 °C/0.4-0.5 mmHg
Density 0.875 g/mL at 25 °C
refractive index 1.445
Flash point 73-77°C/0.5mm
storage temp. 2-8°C

SAFETY

Risk and Safety Statements

WGK Germany  3
NFPA 704
0
0 0

trans-1-Hepten-1-ylboronic acid pinacol ester price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 662992 trans-1-Hepten-1-ylboronic acid pinacol ester 97% 169339-75-7 5g $165 2023-06-20 Buy
TRC T705680 trans-1-HeptenylboronicAcidPinacolEster 169339-75-7 500mg $75 2021-12-16 Buy
American Custom Chemicals Corporation BOR0000838 TRANS-1-HEPTENYLBORONIC ACID PINACOL ESTER 95.00% 169339-75-7 5G $241.5 2021-12-16 Buy
Crysdot CD13020813 (E)-2-(Hept-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 95+% 169339-75-7 10g $323 2021-12-16 Buy
Alichem 169339757 (E)-2-(Hept-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 169339-75-7 10g $400 2021-12-16 Buy
Product number Packaging Price Buy
662992 5g $165 Buy
T705680 500mg $75 Buy
BOR0000838 5G $241.5 Buy
CD13020813 10g $323 Buy
169339757 10g $400 Buy

trans-1-Hepten-1-ylboronic acid pinacol ester Chemical Properties,Uses,Production

Uses

Substrate used in a palladium-catalyzed cross-coupling with olefins providing substituted 1,3-dienes.

Uses

trans-1-Hepten-1-ylboronic acid pinacol ester can be used in a palladium-catalyzed cross-coupling with olefins providing substituted 1,3-dienes.

trans-1-Hepten-1-ylboronic acid pinacol ester Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 35)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
Wuhan Chemwish Technology Co., Ltd
027-67849912 sales@chemwish.com CHINA 10828 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131980 58
Meryer (Shanghai) Chemical Technology Co., Ltd. 021-61259108 18621169109 market03@meryer.com China 40240 62
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30132 84
Energy Chemical 021-021-58432009 400-005-6266 sales8178@energy-chemical.com China 44700 61
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35906 56
Shanghai Hanhong Scientific Co.,Ltd. 021-021-64543801 13764082696 2355241799@qq.com China 42982 64
Shanghai Shenyue Chemical Co., Ltd. 021-021-52212593 15300879511 sales@nuohey.com China 5085 60
TRANS-1-HEPTENYLBORONIC ACID PINACOL ESTER TRANS-1-HEPTENYL-1-BORONIC ACID PINACOL ESTER TRANS-4,4,5,5-TETRAMETHYL-2-HEPT-1-ENYL-1,3,2-DIOXABOROLANE E-2-(1-HEPTENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE 1-HEPTENYL-1-BORONIC ACID, PINACOL ESTER trans-1-Heptenylboronic acid pinacol ester, E-2-(1-Heptenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane trans-1-Hepten-1-ylboronic acid pinacol ester, 97% trans-1-Hepten-1-ylboronic acid pinacol ester 97% 2-[(E)-hept-1-enyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (E)-2-(Hept-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 1,3,2-Dioxaborolane, 2-(1E)-1-hepten-1-yl-4,4,5,5-tetramethyl- 169339-75-7 C13H25BO2 Boronic Acids and Derivatives Boronate Esters Organometallic Reagents Alkenyl Alkenyl Boronate Esters Boronate Esters Boronic Acids and Derivatives Chemical Synthesis Organometallic Reagents Heterocyclic Compounds