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1201905-61-4

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1201905-61-4 Usage

Uses

trans-2-Ethoxyvinylboronic acid pinacol ester is a boronic ester commonly used in Suzuki-Miyaura cross-coupling.This reaction is a key step to synthesize:Azaindole and diazaindoles from chloroamino-N-heterocycles.Doryanine and its derivatives from 2-bromobenzoic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 1201905-61-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,9,0 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1201905-61:
(9*1)+(8*2)+(7*0)+(6*1)+(5*9)+(4*0)+(3*5)+(2*6)+(1*1)=104
104 % 10 = 4
So 1201905-61-4 is a valid CAS Registry Number.

1201905-61-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H33367)  trans-2-Ethoxyethenyl-1-boronic acid pinacol ester, 98%   

  • 1201905-61-4

  • 1g

  • 2070.0CNY

  • Detail
  • Alfa Aesar

  • (H33367)  trans-2-Ethoxyethenyl-1-boronic acid pinacol ester, 98%   

  • 1201905-61-4

  • 5g

  • 5579.0CNY

  • Detail

1201905-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-Ethoxyethene-2-boronic acid pinacol ester

1.2 Other means of identification

Product number -
Other names 2-propenyl cyclohexan-1-one

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:1201905-61-4 SDS

1201905-61-4Relevant articles and documents

Concise synthesis of new bridged-nicotine analogues

Crestey, Franois,Hooyberghs, Geert,Kristensen, Jesper L.

, p. 1417 - 1421 (2012)

This study describes a very efficient strategy for the synthesis of two new bridged-nicotine analogues. Starting from either 4- or 3-chloropyridine the desired tricyclic ring systems are accessed in just three steps in 23% and 40% overall yield, respectively.

1H-PYRROLO[2,3-B]PYRIDINE DERIVATIVES AS BCL-2 INHIBITORS FOR THE TREATMENT OF NEOPLASTIC AND AUTOIMMUNE DISEASES

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Page/Page column 173; 178, (2021/07/02)

The present invention relates to lH-pyrrolo[2,3-b]pyridine derivatives and related compounds as BCL-2 inhibitors for treating neoplastic, autoimmune or neurodegenerative diseases. The present description discloses the synthesis and characterisation of exemplary compounds as well as pharmacological data thereof (e.g. pages 162 to 233; examples 1 to 8; table; compound examples cpd-1 to cpd-135; biological examples 1 to 4).

ISOQUINOLINE DERIVATIVES AS PERK INHIBITORS

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Page/Page column 120, (2018/02/17)

The invention is directed to substituted isoquinoline derivatives and uses thereof. Specifically, the invention is directed to compounds according to Formula I and the use of compounds of Formula (I) in treating disease states: (I) wherein R1,

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