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(Z)-tert-butyldimethyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-3-enyloxy)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116376-35-3

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116376-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116376-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116376-35:
(8*1)+(7*1)+(6*6)+(5*3)+(4*7)+(3*6)+(2*3)+(1*5)=123
123 % 10 = 3
So 116376-35-3 is a valid CAS Registry Number.

116376-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-tert-butyldimethyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-3-enyloxy)silane

1.2 Other means of identification

Product number -
Other names -

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:116376-35-3 SDS

116376-35-3Downstream Products

116376-35-3Relevant academic research and scientific papers

Rhodium-catalyzed dehydrogenative borylation of aliphatic terminal alkenes with pinacolborane

Morimoto, Masao,Miura, Tomoya,Murakami, Masahiro

supporting information, p. 12659 - 12663 (2015/10/28)

Aliphatic terminal alkenes react with pinacolborane at ambient temperature to afford dehydrogenative borylation compounds as the major product when iPr-Foxap is used as the ligand with cationic rhodium(I) in the presence of norbornene, which acts as the s

Stereoselective synthesis of (E)-vinylboronic esters via a Zr mediated hydroboration of alkynes

-

Page/Page column 3, (2008/06/13)

There is herein provided a process for Zr-mediated hydroboration of alkynes which offers (E)-vinylboronic esters in high yield with stereoselectivity and regioselectivity.

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