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2-Butoxy-1,3,2-benzodioxaborole is an organic compound with the chemical formula C11H13BO3. It is a colorless to pale yellow liquid and is soluble in organic solvents. 2-Butoxy-1,3,2-benzodioxaborole is a versatile reagent in organic synthesis, particularly useful for the formation of carbon-carbon bonds through the borylation of alkenes and alkynes. It is also employed in the synthesis of various heterocyclic compounds and as a protecting group in the preparation of complex organic molecules. The compound is known for its stability and selectivity in reactions, making it a valuable tool in the field of organic chemistry.

3488-87-7

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3488-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3488-87-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3488-87:
(6*3)+(5*4)+(4*8)+(3*8)+(2*8)+(1*7)=117
117 % 10 = 7
So 3488-87-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BO3/c1-2-3-8-12-11-13-9-6-4-5-7-10(9)14-11/h4-7H,2-3,8H2,1H3

3488-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butoxy-1,3,2-benzodioxaborole

1.2 Other means of identification

Product number -
Other names Borsaeure-butylester-o-phenylenester

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:3488-87-7 SDS

3488-87-7Relevant academic research and scientific papers

Mild metal-free syn-stereoselective ring opening of activated epoxides and aziridines with aryl borates

Pineschi, Mauro,Bertolini, Ferruccio,Haak, Robert M.,Crotti, Paolo,Macchia, Franco

, p. 1426 - 1428 (2007/10/03)

A conceptually new, simple and practical method for the syn-nucleophilic displacement of aryl and vinyl epoxides and aryl aziridines with (substituted) phenols, using aryl borates as activating nucleophiles under neutral conditions, is reported. The Royal Society of Chemistry 2005.

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