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

Product Name: 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-HEPTENYLBORONIC 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-
CBNumber: CB6776048
Molecular Formula: C13H25BO2
Formula Weight: 224.15
MOL File: 169339-75-7.mol

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

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

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Safety

WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 662992
Product name: trans-1-Hepten-1-ylboronic acid pinacol ester
Purity: 97%
Packaging: 5g
Price: $165
Updated: 2023/06/20

TRC

Product number: T705680
Product name: trans-1-HeptenylboronicAcidPinacolEster
Packaging: 500mg
Price: $75
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: BOR0000838
Product name: TRANS-1-HEPTENYLBORONIC ACID PINACOL ESTER
Purity: 95.00%
Packaging: 5G
Price: $241.5
Updated: 2021/12/16

Crysdot

Product number: CD13020813
Product name: (E)-2-(Hept-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity: 95+%
Packaging: 10g
Price: $323
Updated: 2021/12/16

Alichem

Product number: 169339757
Product name: (E)-2-(Hept-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Packaging: 10g
Price: $400
Updated: 2021/12/16

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trans-1-Hepten-1-ylboronic acid pinacol ester Chemical Properties,Usage,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

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

China 21 Germany 2 Switzerland 1 United Kingdom 2 United States 8 Global 34

CARBONE SCIENTIFIC CO.,LTD

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Email: sales@carbonesci.com
Country: United Kingdom
ProdList: 6666
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UK GREEN SCIENTIFIC CO.,LIMITED

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ProdList: 6098
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169339-75-7, trans-1-Hepten-1-ylboronic acid pinacol esterRelated Search:

1-HEPTENE 1-CIS-1,2-BIS(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)HEPTENE TRANS-4,4,5,5-TETRAMETHYL-2-OCT-1-ENYL-1,3,2-DIOXABOROLANE trans-1-Hepten-1-ylboronic acid pinacol ester METHYL 4 4 5 5-TETRAMETHYL-ALPHA-(1-(4 1-Cyclohepten-1yl boronic acid pinacol ester TRANS-2-(3-CYCLOPENTYLPROPEN-1-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE TRANS-2-(1-CYCLOHEXENYL)VINYLBORONIC ACID PINACOL ESTER 1-VINYL-(CIS-1,2-BIS(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL))CYCLOHEXAN-1-OL

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-

TRANS-HEPTENYLBORONIC ACID, PINACOL ESTER

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