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Benzenemethanol, 4-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

443776-91-8

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443776-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 443776-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,7,7 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 443776-91:
(8*4)+(7*4)+(6*3)+(5*7)+(4*7)+(3*6)+(2*9)+(1*1)=178
178 % 10 = 8
So 443776-91-8 is a valid CAS Registry Number.

443776-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanol

1.2 Other means of identification

Product number -
Other names [4-Methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanol

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:443776-91-8 SDS

443776-91-8Relevant academic research and scientific papers

MACROCYCLIC PYRIDAZINONE DERIVATIVES

-

Page/Page column 60, (2014/08/20)

The present invention relates to compounds of formula (I) Wherein R1, R2, R3, R4, L and Z have the meaning given in claim 1, and their use in the prophylaxis and treatment of diseases.

The conversion of phenols to the corresponding aryl halides under mild conditions

Thompson, Alicia L. S.,Kabalka, George W.,Akula, Murthy R.,Huffman, John W.

, p. 547 - 550 (2007/10/03)

Mild, novel procedures have been developed for the syntheses of aryl halides from the corresponding phenols in modest to good yields via boronate ester intermediates.

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